Database

BC-TFdb Transcription factors drivers in Breast Cancer Database

id TP53 VariantID Class ConseqType AA AAcoord sift_sort SIFT polyphen_sort polyphen_class PolyPhen cadd_sort cadd_class CADD
1 id Variant ID Class Conseq. Type AA AA coord sift_sort SIFT polyphen_sort polyphen_class PolyPhen cadd_sort cadd_class CADD
2 TP53 rs1567535890 SNP missense variant H/Y 342 292 benign 0.291 2001 likely benign 2
3 TP53 rs764432741 SNP missense variant S/P 341 251 benign 0.25 1 likely benign 0
4 TP53 rs1378564917 SNP missense variant G/E 340 970 probably damaging 0.969 2001 likely benign 2
5 TP53 rs753947213 SNP missense variant G/R 340 980 probably damaging 0.979 4001 likely benign 4
6 TP53 rs554512119 SNP missense variant G/R 339 1 benign 0 1 likely benign 0
7 TP53 rs554512119 SNP missense variant G/S 339 1 benign 0 1 likely benign 0
8 TP53 rs144366923 SNP missense variant R/T 337 1 0 96 benign 0.095 1001 likely benign 1
9 TP53 rs1483708811 SNP missense variant P/L 335 131 0.13 1 benign 0 5001 likely benign 5
10 TP53 rs1486846348 SNP missense variant T/I 333 71 0.07 106 benign 0.105 2001 likely benign 2
11 TP53 rs868721462 SNP missense variant T/A 333 161 0.16 13 benign 0.012 6001 likely benign 6
12 TP53 rs1207613599 SNP missense variant K/R 332 31 0.03 1 benign 0 3001 likely benign 3
13 TP53 rs11575996 SNP missense variant Q/H 331 11 0.01 252 benign 0.251 33001 likely deleterious 33
14 TP53 rs1064795056 SNP missense variant Q/R 331 41 0.04 787 possibly damaging 0.786 24001 likely benign 24
15 TP53 rs969930693 SNP missense variant T/I 329 31 0.03 323 benign 0.322 21001 likely benign 21
16 TP53 rs1000256867 SNP missense variant E/D 326 111 0.11 423 benign 0.422 21001 likely benign 21
17 TP53 rs1000256867 SNP missense variant E/D 326 111 0.11 423 benign 0.422 21001 likely benign 21
18 TP53 rs121912659 SNP missense variant G/V 325 171 0.17 256 benign 0.255 18001 likely benign 18
19 TP53 rs121912659 SNP missense variant G/E 325 1001 1 4 benign 0.003 8001 likely benign 8
20 TP53 rs863224500 SNP missense variant G/R 325 331 0.33 19 benign 0.018 23001 likely benign 23
21 TP53 rs1177881399 SNP missense variant D/G 324 1 0 891 possibly damaging 0.89 32001 likely deleterious 32
22 TP53 rs1064794810 SNP missense variant D/Y 324 1 0 986 probably damaging 0.985 26001 likely benign 26
23 TP53 rs1064794810 SNP missense variant D/H 324 1 0 971 probably damaging 0.97 25001 likely benign 25
24 TP53 rs1064794810 SNP missense variant D/N 324 51 0.05 300 benign 0.299 23001 likely benign 23
25 TP53 rs1432281680 SNP missense variant L/V 323 511 0.51 50 benign 0.049 12001 likely benign 12
26 TP53 rs863224687 SNP missense variant P/S 322 351 0.35 38 benign 0.037 17001 likely benign 17
27 TP53 rs863224687 SNP missense variant P/T 322 81 0.08 30 benign 0.029 17001 likely benign 17
28 TP53 rs1555524975 SNP missense variant P/L 318 11 0.01 463 possibly damaging 0.462 19001 likely benign 19
29 TP53 rs1060501199 SNP missense variant Q/H 317 101 0.1 606 possibly damaging 0.605 14001 likely benign 14
30 TP53 rs1159579789 SNP missense variant Q/R 317 441 0.44 143 benign 0.142 9001 likely benign 9
31 TP53 rs764735889 SNP missense variant Q/K 317 1001 1 8 benign 0.007 9001 likely benign 9
32 TP53 rs1555524979 SNP missense variant P/L 316 41 0.04 251 benign 0.25 22001 likely benign 22
33 TP53 rs772773208 SNP missense variant P/T 316 411 0.41 21 benign 0.02 19001 likely benign 19
34 TP53 rs762620193 SNP missense variant S/T 315 171 0.17 21 benign 0.02 16001 likely benign 16
35 TP53 rs751440465 SNP missense variant S/F 314 111 0.11 112 benign 0.111 22001 likely benign 22
36 TP53 rs1367492395 SNP missense variant S/R 313 41 0.04 569 possibly damaging 0.568 18001 likely benign 18
37 TP53 rs145151284 SNP missense variant T/S 312 261 0.26 20 benign 0.019 13001 likely benign 13
38 TP53 rs56184981 SNP missense variant N/S 311 1001 1 2 benign 0.001 1 likely benign 0
39 TP53 rs56184981 SNP missense variant N/T 311 811 0.81 1 benign 0 1 likely benign 0
40 TP53 rs1555525007 SNP missense variant N/H 311 161 0.16 8 benign 0.007 4001 likely benign 4
41 TP53 rs876660829 SNP missense variant N/K 310 601 0.6 1 benign 0 1 likely benign 0
42 TP53 rs876660829 SNP missense variant N/K 310 601 0.6 1 benign 0 1 likely benign 0
43 TP53 rs1555525012 SNP missense variant P/S 309 361 0.36 51 benign 0.05 17001 likely benign 17
44 TP53 rs1457582183 SNP missense variant A/V 307 81 0.08 107 benign 0.106 10001 likely benign 10
45 TP53 rs1457582183 SNP missense variant A/G 307 241 0.24 163 benign 0.162 10001 likely benign 10
46 TP53 rs1048095040 SNP missense variant R/Q 306 41 0.04 612 possibly damaging 0.611 22001 likely benign 22
47 TP53 rs587782654 SNP missense variant T/A 304 351 0.35 12 benign 0.011 14001 likely benign 14
48 TP53 rs876658714 SNP missense variant S/N 303 121 0.12 30 benign 0.029 15001 likely benign 15
49 TP53 rs587782391 SNP missense variant S/G 303 271 0.27 18 benign 0.017 20001 likely benign 20
50 TP53 rs1060501202 SNP missense variant G/E 302 151 0.15 153 benign 0.152 15001 likely benign 15
51 TP53 rs863224686 SNP missense variant G/R 302 131 0.13 42 benign 0.041 10001 likely benign 10
52 TP53 rs1555525067 SNP missense variant P/L 301 41 0.04 13 benign 0.012 12001 likely benign 12
53 TP53 rs909643864 SNP missense variant P/L 300 11 0.01 382 benign 0.381 20001 likely benign 20
54 TP53 rs201744589 SNP missense variant E/Q 298 141 0.14 39 benign 0.038 1 likely benign 0
55 TP53 rs201744589 SNP missense variant E/K 298 231 0.23 8 benign 0.007 1001 likely benign 1
56 TP53 rs876659477 SNP missense variant H/R 297 211 0.21 1 benign 0 4001 likely benign 4
57 TP53 rs483352696 SNP missense variant H/R 296 531 0.53 1 benign 0 1001 likely benign 1
58 TP53 rs672601296 SNP missense variant H/Y 296 41 0.04 16 benign 0.015 3001 likely benign 3
59 TP53 rs751713111 SNP missense variant P/L 295 201 0.2 8 benign 0.007 11001 likely benign 11
60 TP53 rs751713111 SNP missense variant P/R 295 151 0.15 21 benign 0.02 10001 likely benign 10
61 TP53 rs1131691006 SNP missense variant P/S 295 411 0.41 2 benign 0.001 1 likely benign 0
62 TP53 rs1305324490 SNP missense variant E/D 294 181 0.18 57 benign 0.056 3001 likely benign 3
63 TP53 rs587780076 SNP missense variant G/W 293 161 0.16 30 benign 0.029 18001 likely benign 18
64 TP53 rs587780076 SNP missense variant G/R 293 461 0.46 486 possibly damaging 0.485 15001 likely benign 15
65 TP53 rs121912663 SNP missense variant K/I 292 1 0 744 possibly damaging 0.743 23001 likely benign 23
66 TP53 rs121912663 SNP missense variant K/R 292 161 0.16 32 benign 0.031 21001 likely benign 21
67 TP53 rs372613518 SNP missense variant K/N 291 71 0.07 146 benign 0.145 18001 likely benign 18
68 TP53 rs781490101 SNP missense variant K/R 291 11 0.01 158 benign 0.157 25001 likely benign 25
69 TP53 rs1555525126 SNP missense variant K/E 291 191 0.19 696 possibly damaging 0.695 24001 likely benign 24
70 TP53 rs1060501205 substitution missense variant RK/RQ 290 - -
71 TP53 rs55819519 SNP missense variant R/L 290 61 0.06 16 benign 0.015 3001 likely benign 3
72 TP53 rs55819519 SNP missense variant R/P 290 11 0.01 864 possibly damaging 0.863 13001 likely benign 13
73 TP53 rs55819519 SNP missense variant R/H 290 351 0.35 6 benign 0.005 1001 likely benign 1
74 TP53 rs770374782 SNP missense variant R/C 290 1 0 878 possibly damaging 0.877 26001 likely benign 26
75 TP53 rs770374782 SNP missense variant R/G 290 51 0.05 647 possibly damaging 0.646 22001 likely benign 22
76 TP53 rs1555525154 SNP missense variant L/V 289 41 0.04 1 benign 0 12001 likely benign 12
77 TP53 rs748891343 SNP missense variant E/D 287 651 0.65 28 benign 0.027 4001 likely benign 4
78 TP53 rs587782006 SNP missense variant E/K 287 21 0.02 224 benign 0.223 23001 likely benign 23
79 TP53 rs1057519985 SNP missense variant E/V 286 1 0 710 possibly damaging 0.709 32001 likely deleterious 32
80 TP53 rs1057519985 SNP missense variant E/G 286 1 0 991 probably damaging 0.99 32001 likely deleterious 32
81 TP53 rs1057519985 SNP missense variant E/A 286 1 0 985 probably damaging 0.984 31001 likely deleterious 31
82 TP53 rs786201059 SNP missense variant E/Q 286 1 0 984 probably damaging 0.983 27001 likely benign 27
83 TP53 rs786201059 SNP missense variant E/K 286 1 0 978 probably damaging 0.977 29001 likely benign 29
84 TP53 rs121912667 SNP missense variant E/V 285 1 0 984 probably damaging 0.983 29001 likely benign 29
85 TP53 rs112431538 SNP missense variant E/K 285 1 0 958 probably damaging 0.957 28001 likely benign 28
86 TP53 rs863224685 SNP missense variant T/I 284 21 0.02 364 benign 0.363 26001 likely benign 26
87 TP53 rs1204379654 SNP missense variant T/S 284 161 0.16 77 benign 0.076 23001 likely benign 23
88 TP53 rs1204379654 SNP missense variant T/P 284 1 0 930 probably damaging 0.929 26001 likely benign 26
89 TP53 rs371409680 SNP missense variant R/P 283 1 0 952 probably damaging 0.951 27001 likely benign 27
90 TP53 rs371409680 SNP missense variant R/H 283 41 0.04 103 benign 0.102 26001 likely benign 26
91 TP53 rs149633775 SNP missense variant R/C 283 51 0.05 128 benign 0.127 23001 likely benign 23
92 TP53 rs149633775 SNP missense variant R/G 283 21 0.02 136 benign 0.135 24001 likely benign 24
93 TP53 rs149633775 SNP missense variant R/S 283 41 0.04 451 possibly damaging 0.45 22001 likely benign 22
94 TP53 rs730882008 SNP missense variant R/L 282 1 0 710 possibly damaging 0.709 28001 likely benign 28
95 TP53 rs730882008 SNP missense variant R/P 282 1 0 997 probably damaging 0.996 29001 likely benign 29
96 TP53 rs730882008 SNP missense variant R/Q 282 1 0 963 probably damaging 0.962 28001 likely benign 28
97 TP53 rs28934574 SNP missense variant R/W 282 1 0 1000 probably damaging 0.999 31001 likely deleterious 31
98 TP53 rs28934574 SNP missense variant R/G 282 21 0.02 631 possibly damaging 0.63 27001 likely benign 27
99 TP53 rs1057519984 SNP missense variant D/E 281 1 0 516 possibly damaging 0.515 24001 likely benign 24
100 TP53 rs1057519984 SNP missense variant D/E 281 1 0 516 possibly damaging 0.515 24001 likely benign 24
101 TP53 rs587781525 SNP missense variant D/V 281 1 0 978 probably damaging 0.977 29001 likely benign 29
102 TP53 rs587781525 SNP missense variant D/G 281 11 0.01 995 probably damaging 0.994 31001 likely deleterious 31
103 TP53 rs587781525 SNP missense variant D/A 281 1 0 983 probably damaging 0.982 31001 likely deleterious 31
104 TP53 rs764146326 SNP missense variant D/Y 281 1 0 994 probably damaging 0.993 28001 likely benign 28
105 TP53 rs764146326 SNP missense variant D/H 281 51 0.05 603 possibly damaging 0.602 24001 likely benign 24
106 TP53 rs764146326 SNP missense variant D/N 281 11 0.01 976 probably damaging 0.975 28001 likely benign 28
107 TP53 rs1567547687 SNP missense variant R/S 280 21 0.02 762 possibly damaging 0.761 24001 likely benign 24
108 TP53 rs121912660 SNP missense variant R/I 280 1 0 980 probably damaging 0.979 30001 likely deleterious 30
109 TP53 rs121912660 SNP missense variant R/T 280 1 0 967 probably damaging 0.966 28001 likely benign 28
110 TP53 rs121912660 SNP missense variant R/K 280 31 0.03 589 possibly damaging 0.588 27001 likely benign 27
111 TP53 rs753660142 SNP missense variant R/G 280 1 0 967 probably damaging 0.966 28001 likely benign 28
112 TP53 rs1064793881 SNP missense variant G/E 279 1 0 1001 probably damaging 1 25001 likely benign 25
113 TP53 rs1555525248 SNP missense variant G/R 279 21 0.02 1000 probably damaging 0.999 33001 likely deleterious 33
114 TP53 rs876659802 SNP missense variant P/L 278 21 0.02 997 probably damaging 0.996 32001 likely deleterious 32
115 TP53 rs876659802 SNP missense variant P/R 278 1 0 1001 probably damaging 1 29001 likely benign 29
116 TP53 rs876659802 SNP missense variant P/H 278 1 0 1000 probably damaging 0.999 29001 likely benign 29
117 TP53 rs17849781 SNP missense variant P/S 278 21 0.02 965 probably damaging 0.964 28001 likely benign 28
118 TP53 rs17849781 SNP missense variant P/A 278 1 0 975 probably damaging 0.974 27001 likely benign 27
119 TP53 rs17849781 SNP missense variant P/T 278 1 0 995 probably damaging 0.994 28001 likely benign 28
120 TP53 rs763098116 SNP missense variant C/F 277 1 0 978 probably damaging 0.977 27001 likely benign 27
121 TP53 rs763098116 SNP missense variant C/Y 277 1 0 978 probably damaging 0.977 26001 likely benign 26
122 TP53 rs1064795369 SNP missense variant C/G 277 21 0.02 983 probably damaging 0.982 28001 likely benign 28
123 TP53 rs1064795369 SNP missense variant C/R 277 1 0 992 probably damaging 0.991 31001 likely deleterious 31
124 TP53 rs786202082 SNP missense variant A/G 276 1 0 912 probably damaging 0.911 29001 likely benign 29
125 TP53 rs786202082 SNP missense variant A/D 276 1 0 970 probably damaging 0.969 29001 likely benign 29
126 TP53 rs1131691029 SNP missense variant A/P 276 21 0.02 988 probably damaging 0.987 27001 likely benign 27
127 TP53 rs1555525279 SNP missense variant C/W 275 1 0 1000 probably damaging 0.999 29001 likely benign 29
128 TP53 rs863224451 SNP missense variant C/F 275 1 0 992 probably damaging 0.991 27001 likely benign 27
129 TP53 rs863224451 SNP missense variant C/S 275 1 0 990 probably damaging 0.989 29001 likely benign 29
130 TP53 rs863224451 SNP missense variant C/Y 275 1 0 998 probably damaging 0.997 27001 likely benign 27
131 TP53 rs1057519983 SNP missense variant C/R 275 1 0 998 probably damaging 0.997 31001 likely deleterious 31
132 TP53 rs1057520006 SNP missense variant V/G 274 1 0 999 probably damaging 0.998 27001 likely benign 27
133 TP53 rs1057520006 SNP missense variant V/A 274 1 0 885 possibly damaging 0.884 27001 likely benign 27
134 TP53 rs1057520006 SNP missense variant V/D 274 1 0 997 probably damaging 0.996 28001 likely benign 28
135 TP53 rs1057520005 SNP missense variant V/F 274 41 0.04 315 benign 0.314 21001 likely benign 21
136 TP53 rs1057520005 SNP missense variant V/L 274 41 0.04 59 benign 0.058 16001 likely benign 16
137 TP53 rs28934576 SNP missense variant R/L 273 1 0 936 probably damaging 0.935 28001 likely benign 28
138 TP53 rs28934576 SNP missense variant R/P 273 1 0 995 probably damaging 0.994 28001 likely benign 28
139 TP53 rs28934576 SNP missense variant R/H 273 91 0.09 304 benign 0.303 24001 likely benign 24
140 TP53 rs121913343 SNP missense variant R/C 273 1 0 994 probably damaging 0.993 31001 likely deleterious 31
141 TP53 rs121913343 SNP missense variant R/G 273 1 0 971 probably damaging 0.97 28001 likely benign 28
142 TP53 rs121913343 SNP missense variant R/S 273 1 0 846 possibly damaging 0.845 27001 likely benign 27
143 TP53 rs876660333 SNP missense variant V/G 272 221 0.22 1000 probably damaging 0.999 25001 likely benign 25
144 TP53 rs876660333 SNP missense variant V/A 272 231 0.23 987 probably damaging 0.986 25001 likely benign 25
145 TP53 rs876660333 SNP missense variant V/E 272 11 0.01 1000 probably damaging 0.999 25001 likely benign 25
146 TP53 rs121912657 SNP missense variant V/L 272 11 0.01 869 possibly damaging 0.868 26001 likely benign 26
147 TP53 rs121912657 SNP missense variant V/L 272 11 0.01 869 possibly damaging 0.868 26001 likely benign 26
148 TP53 rs121912657 SNP missense variant V/M 272 1 0 997 probably damaging 0.996 26001 likely benign 26
149 TP53 rs1555525303 substitution missense variant EV/DM 271 - -
150 TP53 rs1567548090 substitution missense variant E/L 271 1 0 1000 probably damaging 0.999 -
151 TP53 rs1060501191 SNP missense variant E/K 271 1 0 987 probably damaging 0.986 29001 likely benign 29
152 TP53 rs1057519987 SNP missense variant F/L 270 61 0.06 921 probably damaging 0.92 31001 likely deleterious 31
153 TP53 rs1057519986 SNP missense variant F/C 270 1 0 1000 probably damaging 0.999 31001 likely deleterious 31
154 TP53 rs1057519986 SNP missense variant F/S 270 1 0 1000 probably damaging 0.999 32001 likely deleterious 32
155 TP53 rs1057519988 SNP missense variant F/V 270 21 0.02 978 probably damaging 0.977 29001 likely benign 29
156 TP53 rs1057519988 SNP missense variant F/L 270 61 0.06 921 probably damaging 0.92 31001 likely deleterious 31
157 TP53 rs1057519988 SNP missense variant F/I 270 1 0 747 possibly damaging 0.746 29001 likely benign 29
158 TP53 rs587780075 SNP missense variant R/P 267 1 0 997 probably damaging 0.996 32001 likely deleterious 32
159 TP53 rs587780075 SNP missense variant R/Q 267 1 0 966 probably damaging 0.965 32001 likely deleterious 32
160 TP53 rs55832599 SNP missense variant R/W 267 41 0.04 646 possibly damaging 0.645 26001 likely benign 26
161 TP53 rs193920774 SNP missense variant G/V 266 1 0 982 probably damaging 0.981 29001 likely benign 29
162 TP53 rs193920774 SNP missense variant G/E 266 1 0 864 possibly damaging 0.863 28001 likely benign 28
163 TP53 rs1057519990 SNP missense variant G/R 266 21 0.02 774 possibly damaging 0.773 29001 likely benign 29
164 TP53 rs1057519990 SNP missense variant G/R 266 21 0.02 774 possibly damaging 0.773 29001 likely benign 29
165 TP53 rs879253942 SNP missense variant L/P 265 1 0 999 probably damaging 0.998 32001 likely deleterious 32
166 TP53 rs1555525353 SNP missense variant L/P 264 101 0.1 150 benign 0.149 23001 likely benign 23
167 TP53 rs770598448 SNP missense variant N/K 263 331 0.33 6 benign 0.005 1 likely benign 0
168 TP53 rs72661119 SNP missense variant N/D 263 231 0.23 7 benign 0.006 21001 likely benign 21
169 TP53 rs72661119 SNP missense variant N/H 263 131 0.13 22 benign 0.021 21001 likely benign 21
170 TP53 rs1131691025 SNP missense variant G/V 262 1 0 978 probably damaging 0.977 26001 likely benign 26
171 TP53 rs200579969 SNP missense variant G/C 262 1 0 997 probably damaging 0.996 32001 likely deleterious 32
172 TP53 rs200579969 SNP missense variant G/S 262 1 0 684 possibly damaging 0.683 33001 likely deleterious 33
173 TP53 rs786203396 SNP missense variant S/T 261 21 0.02 36 benign 0.035 25001 likely benign 25
174 TP53 rs876658916 SNP missense variant S/Y 260 11 0.01 587 possibly damaging 0.586 24001 likely benign 24
175 TP53 rs745425759 SNP missense variant D/V 259 51 0.05 635 possibly damaging 0.634 25001 likely benign 25
176 TP53 rs745425759 SNP missense variant D/G 259 141 0.14 38 benign 0.037 22001 likely benign 22
177 TP53 rs1567548929 SNP missense variant D/Y 259 21 0.02 155 benign 0.154 23001 likely benign 23
178 TP53 rs1060501201 SNP missense variant E/G 258 1 0 1000 probably damaging 0.999 29001 likely benign 29
179 TP53 rs1060501201 SNP missense variant E/A 258 1 0 1000 probably damaging 0.999 28001 likely benign 28
180 TP53 rs121912652 SNP missense variant E/K 258 1 0 998 probably damaging 0.997 27001 likely benign 27
181 TP53 rs28934577 SNP missense variant L/R 257 1 0 1000 probably damaging 0.999 27001 likely benign 27
182 TP53 rs28934577 SNP missense variant L/P 257 1 0 1001 probably damaging 1 27001 likely benign 27
183 TP53 rs28934577 SNP missense variant L/Q 257 1 0 1000 probably damaging 0.999 27001 likely benign 27
184 TP53 rs587781433 SNP missense variant T/A 256 1 0 877 possibly damaging 0.876 24001 likely benign 24
185 TP53 rs587781433 SNP missense variant T/P 256 21 0.02 721 possibly damaging 0.72 25001 likely benign 25
186 TP53 rs876659675 SNP missense variant I/S 255 1 0 996 probably damaging 0.995 27001 likely benign 27
187 TP53 rs876659675 SNP missense variant I/T 255 1 0 994 probably damaging 0.993 25001 likely benign 25
188 TP53 rs876659675 SNP missense variant I/N 255 1 0 999 probably damaging 0.998 27001 likely benign 27
189 TP53 rs1057519995 SNP missense variant I/F 255 101 0.1 986 probably damaging 0.985 24001 likely benign 24
190 TP53 rs1330865474 SNP missense variant I/S 254 1 0 1001 probably damaging 1 26001 likely benign 26
191 TP53 rs746601313 SNP missense variant I/V 254 11 0.01 770 possibly damaging 0.769 24001 likely benign 24
192 TP53 rs1555525465 SNP missense variant T/N 253 1 0 986 probably damaging 0.985 23001 likely benign 23
193 TP53 rs121912653 SNP missense variant L/P 252 1 0 1001 probably damaging 1 27001 likely benign 27
194 TP53 rs878854074 SNP missense variant I/M 251 1 0 997 probably damaging 0.996 24001 likely benign 24
195 TP53 rs730882027 SNP missense variant I/S 251 1 0 996 probably damaging 0.995 28001 likely benign 28
196 TP53 rs730882027 SNP missense variant I/T 251 31 0.03 997 probably damaging 0.996 27001 likely benign 27
197 TP53 rs730882027 SNP missense variant I/N 251 21 0.02 999 probably damaging 0.998 27001 likely benign 27
198 TP53 rs730882007 SNP missense variant I/L 251 1 0 928 probably damaging 0.927 26001 likely benign 26
199 TP53 rs1064794311 SNP missense variant P/L 250 21 0.02 919 probably damaging 0.918 28001 likely benign 28
200 TP53 rs28934571 SNP missense variant R/S 249 1 0 987 probably damaging 0.986 22001 likely benign 22
201 TP53 rs28934571 SNP missense variant R/S 249 1 0 987 probably damaging 0.986 22001 likely benign 22
202 TP53 rs587782329 SNP missense variant R/M 249 1 0 793 possibly damaging 0.792 32001 likely deleterious 32
203 TP53 rs587782329 SNP missense variant R/T 249 1 0 987 probably damaging 0.986 32001 likely deleterious 32
204 TP53 rs587782329 SNP missense variant R/K 249 31 0.03 867 possibly damaging 0.866 32001 likely deleterious 32
205 TP53 rs587782082 SNP missense variant R/W 249 11 0.01 750 possibly damaging 0.749 23001 likely benign 23
206 TP53 rs587782082 SNP missense variant R/G 249 1 0 991 probably damaging 0.99 23001 likely benign 23
207 TP53 rs11540652 SNP missense variant R/L 248 1 0 951 probably damaging 0.95 29001 likely benign 29
208 TP53 rs11540652 SNP missense variant R/P 248 1 0 992 probably damaging 0.991 32001 likely deleterious 32
209 TP53 rs11540652 SNP missense variant R/Q 248 21 0.02 334 benign 0.333 29001 likely benign 29
210 TP53 rs121912651 SNP missense variant R/W 248 1 0 997 probably damaging 0.996 28001 likely benign 28
211 TP53 rs121912651 SNP missense variant R/G 248 21 0.02 515 possibly damaging 0.514 27001 likely benign 27
212 TP53 rs1555525498 substitution missense variant NR/NW 247 - -
213 TP53 rs786201762 SNP missense variant N/I 247 1 0 1001 probably damaging 1 28001 likely benign 28
214 TP53 rs786201762 SNP missense variant N/S 247 1 0 999 probably damaging 0.998 26001 likely benign 26
215 TP53 rs1452189221 SNP missense variant N/D 247 1 0 1000 probably damaging 0.999 28001 likely benign 28
216 TP53 rs1019340046 SNP missense variant M/I 246 11 0.01 913 probably damaging 0.912 26001 likely benign 26
217 TP53 rs587780074 SNP missense variant M/R 246 1 0 1001 probably damaging 1 28001 likely benign 28
218 TP53 rs587780074 SNP missense variant M/T 246 1 0 1001 probably damaging 1 26001 likely benign 26
219 TP53 rs587780074 SNP missense variant M/K 246 1 0 1001 probably damaging 1 28001 likely benign 28
220 TP53 rs483352695 SNP missense variant M/L 246 111 0.11 947 probably damaging 0.946 26001 likely benign 26
221 TP53 rs483352695 SNP missense variant M/V 246 1 0 965 probably damaging 0.964 25001 likely benign 25
222 TP53 rs483352695 SNP missense variant M/L 246 111 0.11 947 probably damaging 0.946 26001 likely benign 26
223 TP53 rs121912656 SNP missense variant G/V 245 1 0 1000 probably damaging 0.999 26001 likely benign 26
224 TP53 rs121912656 SNP missense variant G/A 245 1 0 996 probably damaging 0.995 25001 likely benign 25
225 TP53 rs121912656 SNP missense variant G/D 245 1 0 1000 probably damaging 0.999 26001 likely benign 26
226 TP53 rs28934575 SNP missense variant G/C 245 1 0 1001 probably damaging 1 28001 likely benign 28
227 TP53 rs28934575 SNP missense variant G/R 245 1 0 990 probably damaging 0.989 27001 likely benign 27
228 TP53 rs28934575 SNP missense variant G/S 245 1 0 1000 probably damaging 0.999 27001 likely benign 27
229 TP53 rs985033810 SNP missense variant G/V 244 1 0 1000 probably damaging 0.999 26001 likely benign 26
230 TP53 rs985033810 SNP missense variant G/A 244 1 0 993 probably damaging 0.992 25001 likely benign 25
231 TP53 rs985033810 SNP missense variant G/D 244 21 0.02 934 probably damaging 0.933 26001 likely benign 26
232 TP53 rs1057519989 SNP missense variant G/C 244 1 0 1001 probably damaging 1 28001 likely benign 28
233 TP53 rs1057519989 SNP missense variant G/R 244 1 0 1000 probably damaging 0.999 27001 likely benign 27
234 TP53 rs1057519989 SNP missense variant G/S 244 1 0 999 probably damaging 0.998 27001 likely benign 27
235 TP53 rs730882006 SNP missense variant M/T 243 1 0 979 probably damaging 0.978 26001 likely benign 26
236 TP53 rs786203117 SNP missense variant M/L 243 41 0.04 136 benign 0.135 25001 likely benign 25
237 TP53 rs786203117 SNP missense variant M/V 243 391 0.39 747 possibly damaging 0.746 24001 likely benign 24
238 TP53 rs786203117 SNP missense variant M/L 243 41 0.04 136 benign 0.135 25001 likely benign 25
239 TP53 rs375874539 SNP missense variant C/W 242 1 0 1001 probably damaging 1 28001 likely benign 28
240 TP53 rs121912655 SNP missense variant C/F 242 1 0 1001 probably damaging 1 27001 likely benign 27
241 TP53 rs121912655 SNP missense variant C/S 242 21 0.02 1001 probably damaging 1 28001 likely benign 28
242 TP53 rs121912655 SNP missense variant C/Y 242 1 0 1001 probably damaging 1 27001 likely benign 27
243 TP53 rs1057519982 SNP missense variant C/G 242 1 0 1001 probably damaging 1 29001 likely benign 29
244 TP53 rs1057519982 SNP missense variant C/R 242 1 0 1001 probably damaging 1 31001 likely deleterious 31
245 TP53 rs1057519982 SNP missense variant C/S 242 21 0.02 1001 probably damaging 1 28001 likely benign 28
246 TP53 rs28934573 SNP missense variant S/F 241 1 0 1001 probably damaging 1 27001 likely benign 27
247 TP53 rs28934573 SNP missense variant S/C 241 1 0 1001 probably damaging 1 26001 likely benign 26
248 TP53 rs28934573 SNP missense variant S/Y 241 1 0 1001 probably damaging 1 26001 likely benign 26
249 TP53 rs1057520002 SNP missense variant S/A 241 1 0 1000 probably damaging 0.999 26001 likely benign 26
250 TP53 rs1057520002 SNP missense variant S/P 241 21 0.02 1001 probably damaging 1 27001 likely benign 27
251 TP53 rs764342812 SNP missense variant S/R 240 1 0 1001 probably damaging 1 26001 likely benign 26
252 TP53 rs1567549584 SNP missense variant S/G 240 21 0.02 1001 probably damaging 1 26001 likely benign 26
253 TP53 rs1057522275 SNP missense variant N/K 239 1 0 999 probably damaging 0.998 24001 likely benign 24
254 TP53 rs1057519999 SNP missense variant N/S 239 31 0.03 786 possibly damaging 0.785 26001 likely benign 26
255 TP53 rs1057519999 SNP missense variant N/T 239 1 0 990 probably damaging 0.989 27001 likely benign 27
256 TP53 rs876660807 SNP missense variant N/D 239 11 0.01 992 probably damaging 0.991 28001 likely benign 28
257 TP53 rs193920789 SNP missense variant C/W 238 1 0 1001 probably damaging 1 24001 likely benign 24
258 TP53 rs730882005 SNP missense variant C/F 238 1 0 1001 probably damaging 1 29001 likely benign 29
259 TP53 rs730882005 SNP missense variant C/S 238 1 0 1001 probably damaging 1 27001 likely benign 27
260 TP53 rs730882005 SNP missense variant C/Y 238 1 0 1001 probably damaging 1 27001 likely benign 27
261 TP53 rs1057519981 SNP missense variant C/G 238 1 0 1001 probably damaging 1 29001 likely benign 29
262 TP53 rs1057519981 SNP missense variant C/R 238 1 0 1001 probably damaging 1 29001 likely benign 29
263 TP53 rs1057519981 SNP missense variant C/S 238 1 0 1001 probably damaging 1 27001 likely benign 27
264 TP53 rs587782664 SNP missense variant M/I 237 1 0 661 possibly damaging 0.66 26001 likely benign 26
265 TP53 rs587782664 SNP missense variant M/I 237 1 0 661 possibly damaging 0.66 26001 likely benign 26
266 TP53 rs587782664 SNP missense variant M/I 237 1 0 661 possibly damaging 0.66 26001 likely benign 26
267 TP53 rs765848205 SNP missense variant M/R 237 1 0 987 probably damaging 0.986 32001 likely deleterious 32
268 TP53 rs765848205 SNP missense variant M/T 237 21 0.02 814 possibly damaging 0.813 26001 likely benign 26
269 TP53 rs765848205 SNP missense variant M/K 237 1 0 980 probably damaging 0.979 28001 likely benign 28
270 TP53 rs730882004 SNP missense variant M/V 237 1 0 835 possibly damaging 0.834 25001 likely benign 25
271 TP53 rs730882026 SNP missense variant Y/C 236 1 0 987 probably damaging 0.986 24001 likely benign 24
272 TP53 rs730882026 SNP missense variant Y/S 236 1 0 997 probably damaging 0.996 25001 likely benign 25
273 TP53 rs587782289 SNP missense variant Y/D 236 1 0 999 probably damaging 0.998 29001 likely benign 29
274 TP53 rs587782289 SNP missense variant Y/H 236 1 0 987 probably damaging 0.986 32001 likely deleterious 32
275 TP53 rs587782289 SNP missense variant Y/N 236 1 0 999 probably damaging 0.998 29001 likely benign 29
276 TP53 rs144340710 SNP missense variant N/I 235 1 0 999 probably damaging 0.998 27001 likely benign 27
277 TP53 rs144340710 SNP missense variant N/S 235 181 0.18 517 possibly damaging 0.516 22001 likely benign 22
278 TP53 rs786204145 SNP missense variant N/Y 235 1 0 999 probably damaging 0.998 29001 likely benign 29
279 TP53 rs587780073 SNP missense variant Y/C 234 1 0 993 probably damaging 0.992 26001 likely benign 26
280 TP53 rs587780073 SNP missense variant Y/S 234 1 0 961 probably damaging 0.96 25001 likely benign 25
281 TP53 rs864622237 SNP missense variant Y/D 234 21 0.02 961 probably damaging 0.96 24001 likely benign 24
282 TP53 rs864622237 SNP missense variant Y/H 234 1 0 990 probably damaging 0.989 27001 likely benign 27
283 TP53 rs864622237 SNP missense variant Y/N 234 1 0 985 probably damaging 0.984 27001 likely benign 27
284 TP53 rs879254233 SNP missense variant H/R 233 21 0.02 59 benign 0.058 25001 likely benign 25
285 TP53 rs587781589 SNP missense variant I/S 232 1 0 911 probably damaging 0.91 31001 likely deleterious 31
286 TP53 rs587781589 SNP missense variant I/T 232 1 0 482 possibly damaging 0.481 29001 likely benign 29
287 TP53 rs1555525562 SNP missense variant I/L 232 31 0.03 90 benign 0.089 20001 likely benign 20
288 TP53 rs1555525564 SNP missense variant T/I 231 21 0.02 974 probably damaging 0.973 29001 likely benign 29
289 TP53 rs1064793603 SNP missense variant C/S 229 381 0.38 47 benign 0.046 22001 likely benign 22
290 TP53 rs1064793603 SNP missense variant C/Y 229 1001 1 66 benign 0.065 17001 likely benign 17
291 TP53 rs1064794312 SNP missense variant C/R 229 291 0.29 921 probably damaging 0.92 24001 likely benign 24
292 TP53 rs970212462 SNP missense variant G/V 226 1 0 608 possibly damaging 0.607 24001 likely benign 24
293 TP53 rs746504075 SNP missense variant V/L 225 231 0.23 28 benign 0.027 22001 likely benign 22
294 TP53 rs746504075 SNP missense variant V/I 225 31 0.03 16 benign 0.015 20001 likely benign 20
295 TP53 rs267605076 SNP missense variant E/D 224 21 0.02 26 benign 0.025 33001 likely deleterious 33
296 TP53 rs1131691028 SNP missense variant E/A 224 1 0 853 possibly damaging 0.852 35001 likely deleterious 35
297 TP53 rs1555525707 SNP missense variant E/K 224 1 0 596 possibly damaging 0.595 28001 likely benign 28
298 TP53 rs138983188 SNP missense variant P/L 223 41 0.04 846 possibly damaging 0.845 25001 likely benign 25
299 TP53 rs138983188 SNP missense variant P/H 223 21 0.02 997 probably damaging 0.996 27001 likely benign 27
300 TP53 rs146340390 SNP missense variant P/L 222 91 0.09 22 benign 0.021 18001 likely benign 18
301 TP53 rs1060501203 SNP missense variant P/S 222 111 0.11 15 benign 0.014 16001 likely benign 16
302 TP53 rs1567551121 SNP missense variant E/A 221 11 0.01 475 possibly damaging 0.474 27001 likely benign 27
303 TP53 rs786201592 SNP missense variant E/K 221 1 0 254 benign 0.253 28001 likely benign 28
304 TP53 rs121912666 SNP missense variant Y/C 220 1 0 997 probably damaging 0.996 32001 likely deleterious 32
305 TP53 rs121912666 SNP missense variant Y/S 220 1 0 838 possibly damaging 0.837 29001 likely benign 29
306 TP53 rs530941076 SNP missense variant Y/D 220 1 0 993 probably damaging 0.992 31001 likely deleterious 31
307 TP53 rs530941076 SNP missense variant Y/H 220 1 0 997 probably damaging 0.996 31001 likely deleterious 31
308 TP53 rs530941076 SNP missense variant Y/N 220 1 0 993 probably damaging 0.992 31001 likely deleterious 31
309 TP53 rs1420675064 SNP missense variant P/L 219 11 0.01 993 probably damaging 0.992 31001 likely deleterious 31
310 TP53 rs879253894 SNP missense variant P/S 219 21 0.02 718 possibly damaging 0.717 28001 likely benign 28
311 TP53 rs1555525743 SNP missense variant V/G 218 1 0 996 probably damaging 0.995 32001 likely deleterious 32
312 TP53 rs878854072 SNP missense variant V/M 218 1 0 990 probably damaging 0.989 25001 likely benign 25
313 TP53 rs35163653 SNP missense variant V/M 217 201 0.2 388 benign 0.387 23001 likely benign 23
314 TP53 rs1057520004 SNP missense variant V/G 216 1 0 999 probably damaging 0.998 32001 likely deleterious 32
315 TP53 rs1057520004 SNP missense variant V/E 216 1 0 999 probably damaging 0.998 31001 likely deleterious 31
316 TP53 rs730882025 SNP missense variant V/L 216 1 0 942 probably damaging 0.941 25001 likely benign 25
317 TP53 rs730882025 SNP missense variant V/L 216 1 0 942 probably damaging 0.941 25001 likely benign 25
318 TP53 rs730882025 SNP missense variant V/M 216 1 0 999 probably damaging 0.998 26001 likely benign 26
319 TP53 rs1057520001 SNP missense variant S/R 215 1 0 1001 probably damaging 1 27001 likely benign 27
320 TP53 rs587782177 SNP missense variant S/I 215 1 0 1001 probably damaging 1 25001 likely benign 25
321 TP53 rs587782177 SNP missense variant S/T 215 1 0 991 probably damaging 0.99 24001 likely benign 24
322 TP53 rs587782177 SNP missense variant S/N 215 1 0 996 probably damaging 0.995 25001 likely benign 25
323 TP53 rs886039484 SNP missense variant S/G 215 11 0.01 998 probably damaging 0.997 26001 likely benign 26
324 TP53 rs886039484 SNP missense variant S/R 215 1 0 1001 probably damaging 1 27001 likely benign 27
325 TP53 rs587781386 SNP missense variant H/Q 214 1001 1 286 benign 0.285 1 likely benign 0
326 TP53 rs1057519992 SNP missense variant H/L 214 11 0.01 959 probably damaging 0.958 27001 likely benign 27
327 TP53 rs1057519992 SNP missense variant H/R 214 41 0.04 942 probably damaging 0.941 26001 likely benign 26
328 TP53 rs1057519992 SNP missense variant H/P 214 11 0.01 993 probably damaging 0.992 27001 likely benign 27
329 TP53 rs876658466 SNP missense variant H/N 214 11 0.01 972 probably damaging 0.971 28001 likely benign 28
330 TP53 rs587778720 SNP missense variant R/L 213 1 0 969 probably damaging 0.968 29001 likely benign 29
331 TP53 rs587778720 SNP missense variant R/P 213 1 0 998 probably damaging 0.997 29001 likely benign 29
332 TP53 rs587778720 SNP missense variant R/Q 213 1 0 789 possibly damaging 0.788 29001 likely benign 29
333 TP53 rs397516436 SNP missense variant R/G 213 21 0.02 987 probably damaging 0.986 24001 likely benign 24
334 TP53 rs1064795766 SNP missense variant F/I 212 391 0.39 183 benign 0.182 16001 likely benign 16
335 TP53 rs1060501198 SNP missense variant T/A 211 1 0 517 possibly damaging 0.516 26001 likely benign 26
336 TP53 rs1060501198 SNP missense variant T/P 211 1 0 952 probably damaging 0.951 28001 likely benign 28
337 TP53 rs1060501200 SNP missense variant N/Y 210 1001 1 587 possibly damaging 0.586 17001 likely benign 17
338 TP53 rs1429743956 SNP missense variant R/G 209 371 0.37 4 benign 0.003 17001 likely benign 17
339 TP53 rs1464727668 SNP missense variant D/V 208 11 0.01 993 probably damaging 0.992 29001 likely benign 29
340 TP53 rs1464727668 SNP missense variant D/G 208 21 0.02 980 probably damaging 0.979 29001 likely benign 29
341 TP53 rs923100890 SNP missense variant D/N 207 21 0.02 30 benign 0.029 22001 likely benign 22
342 TP53 rs1555525804 SNP missense variant L/S 206 81 0.08 27 benign 0.026 16001 likely benign 16
343 TP53 rs1057520007 SNP missense variant Y/F 205 1 0 904 possibly damaging 0.903 26001 likely benign 26
344 TP53 rs1057520007 SNP missense variant Y/C 205 1 0 990 probably damaging 0.989 29001 likely benign 29
345 TP53 rs1057520007 SNP missense variant Y/S 205 1 0 602 possibly damaging 0.601 27001 likely benign 27
346 TP53 rs1057520008 SNP missense variant Y/D 205 1 0 957 probably damaging 0.956 28001 likely benign 28
347 TP53 rs1057520008 SNP missense variant Y/H 205 11 0.01 465 possibly damaging 0.464 26001 likely benign 26
348 TP53 rs1057520008 SNP missense variant Y/N 205 1 0 957 probably damaging 0.956 27001 likely benign 27
349 TP53 rs1260903787 SNP missense variant E/G 204 11 0.01 268 benign 0.267 25001 likely benign 25
350 TP53 rs730882003 SNP missense variant V/L 203 41 0.04 1 benign 0 19001 likely benign 19
351 TP53 rs730882003 SNP missense variant V/L 203 41 0.04 1 benign 0 19001 likely benign 19
352 TP53 rs730882003 SNP missense variant V/M 203 1 0 375 benign 0.374 21001 likely benign 21
353 TP53 rs587778719 SNP missense variant R/L 202 811 0.81 16 benign 0.015 4001 likely benign 4
354 TP53 rs587778719 SNP missense variant R/H 202 661 0.66 4 benign 0.003 3001 likely benign 3
355 TP53 rs587780072 SNP missense variant R/C 202 111 0.11 29 benign 0.028 22001 likely benign 22
356 TP53 rs587780072 SNP missense variant R/G 202 161 0.16 31 benign 0.03 23001 likely benign 23
357 TP53 rs730882024 SNP missense variant L/F 201 701 0.7 34 benign 0.033 7001 likely benign 7
358 TP53 rs1555525857 SNP missense variant G/V 199 1 0 977 probably damaging 0.976 27001 likely benign 27
359 TP53 rs1555525857 SNP missense variant G/E 199 31 0.03 663 possibly damaging 0.662 26001 likely benign 26
360 TP53 rs1567551903 SNP missense variant V/E 197 1 0 997 probably damaging 0.996 29001 likely benign 29
361 TP53 rs786204041 SNP missense variant V/L 197 31 0.03 829 possibly damaging 0.828 24001 likely benign 24
362 TP53 rs786204041 SNP missense variant V/L 197 31 0.03 829 possibly damaging 0.828 24001 likely benign 24
363 TP53 rs786204041 SNP missense variant V/M 197 31 0.03 935 probably damaging 0.934 24001 likely benign 24
364 TP53 rs483352697 SNP missense variant R/L 196 1 0 978 probably damaging 0.977 30001 likely deleterious 30
365 TP53 rs483352697 SNP missense variant R/P 196 1 0 997 probably damaging 0.996 29001 likely benign 29
366 TP53 rs483352697 SNP missense variant R/Q 196 61 0.06 525 possibly damaging 0.524 25001 likely benign 25
367 TP53 rs397516435 SNP missense variant R/G 196 1 0 993 probably damaging 0.992 27001 likely benign 27
368 TP53 rs1057519994 SNP missense variant I/M 195 21 0.02 911 probably damaging 0.91 25001 likely benign 25
369 TP53 rs760043106 SNP missense variant I/S 195 1 0 992 probably damaging 0.991 29001 likely benign 29
370 TP53 rs760043106 SNP missense variant I/T 195 1 0 938 probably damaging 0.937 27001 likely benign 27
371 TP53 rs760043106 SNP missense variant I/N 195 1 0 997 probably damaging 0.996 29001 likely benign 29
372 TP53 rs942158624 SNP missense variant I/F 195 1 0 986 probably damaging 0.985 27001 likely benign 27
373 TP53 rs1057519998 SNP missense variant L/R 194 1 0 1001 probably damaging 1 30001 likely deleterious 30
374 TP53 rs1057519998 SNP missense variant L/P 194 1 0 1001 probably damaging 1 31001 likely deleterious 31
375 TP53 rs1057519998 SNP missense variant L/H 194 1 0 1001 probably damaging 1 29001 likely benign 29
376 TP53 rs587780071 SNP missense variant L/F 194 51 0.05 973 probably damaging 0.972 28001 likely benign 28
377 TP53 rs786201838 SNP missense variant H/L 193 1 0 1001 probably damaging 1 29001 likely benign 29
378 TP53 rs786201838 SNP missense variant H/R 193 1 0 1001 probably damaging 1 27001 likely benign 27
379 TP53 rs786201838 SNP missense variant H/P 193 1 0 1001 probably damaging 1 29001 likely benign 29
380 TP53 rs876658468 SNP missense variant H/Y 193 1 0 1001 probably damaging 1 29001 likely benign 29
381 TP53 rs876658468 SNP missense variant H/D 193 1 0 1001 probably damaging 1 32001 likely deleterious 32
382 TP53 rs876658468 SNP missense variant H/N 193 1 0 1001 probably damaging 1 29001 likely benign 29
383 TP53 rs730882002 SNP missense variant Q/R 192 61 0.06 73 benign 0.072 24001 likely benign 24
384 TP53 rs587778718 SNP missense variant P/L 191 1 0 950 probably damaging 0.949 29001 likely benign 29
385 TP53 rs587778718 SNP missense variant P/R 191 221 0.22 967 probably damaging 0.966 23001 likely benign 23
386 TP53 rs587778718 SNP missense variant P/H 191 1 0 979 probably damaging 0.978 28001 likely benign 28
387 TP53 rs868590738 SNP missense variant P/S 191 41 0.04 228 benign 0.227 23001 likely benign 23
388 TP53 rs876660825 SNP missense variant P/L 190 51 0.05 862 possibly damaging 0.861 27001 likely benign 27
389 TP53 rs876660825 SNP missense variant P/R 190 31 0.03 998 probably damaging 0.997 28001 likely benign 28
390 TP53 rs876660254 SNP missense variant P/T 190 11 0.01 988 probably damaging 0.987 26001 likely benign 26
391 TP53 rs121912665 SNP missense variant A/V 189 31 0.03 771 possibly damaging 0.77 26001 likely benign 26
392 TP53 rs1555525921 SNP missense variant A/S 189 51 0.05 971 probably damaging 0.97 27001 likely benign 27
393 TP53 rs1199893366 SNP missense variant L/P 188 191 0.19 206 benign 0.205 22001 likely benign 22
394 TP53 rs1064795841 SNP missense variant G/D 187 91 0.09 224 benign 0.223 9001 likely benign 9
395 TP53 rs776167460 SNP missense variant G/S 187 141 0.14 334 benign 0.333 23001 likely benign 23
396 TP53 rs375275361 SNP missense variant D/E 186 211 0.21 322 benign 0.321 13001 likely benign 13
397 TP53 rs1060501206 SNP missense variant D/N 186 101 0.1 447 possibly damaging 0.446 22001 likely benign 22
398 TP53 rs150607408 SNP missense variant S/N 185 921 0.92 2 benign 0.001 2001 likely benign 2
399 TP53 rs1060501209 SNP missense variant D/G 184 41 0.04 221 benign 0.22 23001 likely benign 23
400 TP53 rs72661117 SNP missense variant D/N 184 271 0.27 180 benign 0.179 16001 likely benign 16
401 TP53 rs1555525970 SNP missense variant S/L 183 121 0.12 264 benign 0.263 21001 likely benign 21
402 TP53 rs1064796257 SNP missense variant C/W 182 31 0.03 884 possibly damaging 0.883 23001 likely benign 23
403 TP53 rs397514495 SNP missense variant R/L 181 341 0.34 869 possibly damaging 0.868 24001 likely benign 24
404 TP53 rs397514495 SNP missense variant R/H 181 81 0.08 969 probably damaging 0.968 25001 likely benign 25
405 TP53 rs587782596 SNP missense variant R/C 181 131 0.13 308 benign 0.307 24001 likely benign 24
406 TP53 rs587782596 SNP missense variant R/S 181 351 0.35 978 probably damaging 0.977 23001 likely benign 23
407 TP53 rs879253911 SNP missense variant E/K 180 1 0 1001 probably damaging 1 27001 likely benign 27
408 TP53 rs876660821 SNP missense variant H/Q 179 1 0 843 possibly damaging 0.842 12001 likely benign 12
409 TP53 rs876660821 SNP missense variant H/Q 179 1 0 843 possibly damaging 0.842 12001 likely benign 12
410 TP53 rs1057519991 SNP missense variant H/L 179 71 0.07 496 possibly damaging 0.495 22001 likely benign 22
411 TP53 rs1057519991 SNP missense variant H/R 179 1 0 983 probably damaging 0.982 24001 likely benign 24
412 TP53 rs1057519991 SNP missense variant H/P 179 1 0 998 probably damaging 0.997 24001 likely benign 24
413 TP53 rs587780070 SNP missense variant H/Y 179 1 0 995 probably damaging 0.994 27001 likely benign 27
414 TP53 rs587780070 SNP missense variant H/D 179 1 0 995 probably damaging 0.994 27001 likely benign 27
415 TP53 rs587780070 SNP missense variant H/N 179 1 0 995 probably damaging 0.994 26001 likely benign 26
416 TP53 rs1555526001 SNP missense variant H/Q 178 1 0 1000 probably damaging 0.999 24001 likely benign 24
417 TP53 rs1555526004 SNP missense variant H/P 178 1 0 1001 probably damaging 1 29001 likely benign 29
418 TP53 rs1064795203 SNP missense variant H/D 178 1 0 1001 probably damaging 1 25001 likely benign 25
419 TP53 rs1064795203 SNP missense variant H/N 178 411 0.41 1001 probably damaging 1 25001 likely benign 25
420 TP53 rs751477326 SNP missense variant P/L 177 1 0 989 probably damaging 0.988 29001 likely benign 29
421 TP53 rs751477326 SNP missense variant P/R 177 21 0.02 803 possibly damaging 0.802 27001 likely benign 27
422 TP53 rs147002414 SNP missense variant P/S 177 1 0 947 probably damaging 0.946 27001 likely benign 27
423 TP53 rs147002414 SNP missense variant P/T 177 1 0 972 probably damaging 0.971 26001 likely benign 26
424 TP53 rs1057519980 SNP missense variant C/W 176 1 0 1001 probably damaging 1 22001 likely benign 22
425 TP53 rs1567552847 substitution missense variant C/R 176 1 0 1000 probably damaging 0.999 29001 likely benign 29
426 TP53 rs786202962 SNP missense variant C/F 176 1 0 997 probably damaging 0.996 27001 likely benign 27
427 TP53 rs786202962 SNP missense variant C/Y 176 1 0 996 probably damaging 0.995 27001 likely benign 27
428 TP53 rs967461896 SNP missense variant C/G 176 1 0 999 probably damaging 0.998 29001 likely benign 29
429 TP53 rs967461896 SNP missense variant C/R 176 1 0 1000 probably damaging 0.999 29001 likely benign 29
430 TP53 rs967461896 SNP missense variant C/S 176 1 0 933 probably damaging 0.932 27001 likely benign 27
431 TP53 rs28934578 SNP missense variant R/L 175 1 0 707 possibly damaging 0.706 28001 likely benign 28
432 TP53 rs28934578 SNP missense variant R/H 175 81 0.08 110 benign 0.109 23001 likely benign 23
433 TP53 rs138729528 SNP missense variant R/C 175 1 0 296 benign 0.295 32001 likely deleterious 32
434 TP53 rs138729528 SNP missense variant R/G 175 1 0 965 probably damaging 0.964 32001 likely deleterious 32
435 TP53 rs1064796681 SNP missense variant R/K 174 841 0.84 20 benign 0.019 14001 likely benign 14
436 TP53 rs864622115 SNP missense variant R/G 174 1 0 825 possibly damaging 0.824 24001 likely benign 24
437 TP53 rs1057519747 SNP missense variant V/G 173 1 0 1000 probably damaging 0.999 28001 likely benign 28
438 TP53 rs1057519747 SNP missense variant V/A 173 1 0 997 probably damaging 0.996 25001 likely benign 25
439 TP53 rs1057519747 SNP missense variant V/E 173 1 0 999 probably damaging 0.998 26001 likely benign 26
440 TP53 rs876660754 SNP missense variant V/L 173 21 0.02 649 possibly damaging 0.648 24001 likely benign 24
441 TP53 rs876660754 SNP missense variant V/M 173 21 0.02 974 probably damaging 0.973 24001 likely benign 24
442 TP53 rs1131691021 SNP missense variant V/G 172 1 0 988 probably damaging 0.987 25001 likely benign 25
443 TP53 rs1131691021 SNP missense variant V/A 172 21 0.02 964 probably damaging 0.963 24001 likely benign 24
444 TP53 rs1131691043 SNP missense variant V/F 172 1 0 974 probably damaging 0.973 23001 likely benign 23
445 TP53 rs587781845 SNP missense variant E/K 171 21 0.02 992 probably damaging 0.991 24001 likely benign 24
446 TP53 rs779000871 SNP missense variant T/M 170 81 0.08 289 benign 0.288 21001 likely benign 21
447 TP53 rs779000871 SNP missense variant T/R 170 1 0 912 probably damaging 0.911 26001 likely benign 26
448 TP53 rs587780729 SNP missense variant T/A 170 621 0.62 13 benign 0.012 15001 likely benign 15
449 TP53 rs1567553114 SNP missense variant M/R 169 1 0 584 possibly damaging 0.583 23001 likely benign 23
450 TP53 rs867114783 SNP missense variant H/R 168 1 0 904 possibly damaging 0.903 23001 likely benign 23
451 TP53 rs1319163924 SNP missense variant Q/P 167 1 0 775 possibly damaging 0.774 24001 likely benign 24
452 TP53 rs1555526101 SNP missense variant S/L 166 91 0.09 163 benign 0.162 18001 likely benign 18
453 TP53 rs730882001 SNP missense variant Q/K 165 1001 1 1 benign 0 13001 likely benign 13
454 TP53 rs1131691034 SNP missense variant K/N 164 1 0 991 probably damaging 0.99 23001 likely benign 23
455 TP53 rs879254249 SNP missense variant K/E 164 1 0 940 probably damaging 0.939 25001 likely benign 25
456 TP53 rs148924904 SNP missense variant Y/C 163 21 0.02 890 possibly damaging 0.889 24001 likely benign 24
457 TP53 rs786203436 SNP missense variant Y/D 163 1 0 1001 probably damaging 1 26001 likely benign 26
458 TP53 rs786203436 SNP missense variant Y/H 163 1 0 999 probably damaging 0.998 26001 likely benign 26
459 TP53 rs786203436 SNP missense variant Y/N 163 1 0 1001 probably damaging 1 25001 likely benign 25
460 TP53 rs587780069 SNP missense variant I/S 162 31 0.03 453 possibly damaging 0.452 26001 likely benign 26
461 TP53 rs1064795691 SNP missense variant A/D 161 1 0 1001 probably damaging 1 26001 likely benign 26
462 TP53 rs193920817 SNP missense variant A/T 161 11 0.01 1001 probably damaging 1 24001 likely benign 24
463 TP53 rs772354334 SNP missense variant M/I 160 41 0.04 55 benign 0.054 20001 likely benign 20
464 TP53 rs377274728 SNP missense variant M/L 160 81 0.08 11 benign 0.01 18001 likely benign 18
465 TP53 rs377274728 SNP missense variant M/V 160 41 0.04 55 benign 0.054 17001 likely benign 17
466 TP53 rs730882022 substitution missense variant A/F 159 1 0 997 probably damaging 0.996 -
467 TP53 rs1555526131 SNP missense variant A/V 159 1 0 911 probably damaging 0.91 24001 likely benign 24
468 TP53 rs730882000 SNP missense variant A/P 159 1 0 995 probably damaging 0.994 24001 likely benign 24
469 TP53 rs730882000 SNP missense variant A/T 159 111 0.11 333 benign 0.332 22001 likely benign 22
470 TP53 rs1567553501 substitution missense variant R/L 158 1 0 992 probably damaging 0.991 25001 likely benign 25
471 TP53 rs587782144 SNP missense variant R/L 158 1 0 992 probably damaging 0.991 25001 likely benign 25
472 TP53 rs587782144 SNP missense variant R/P 158 1 0 999 probably damaging 0.998 25001 likely benign 25
473 TP53 rs587782144 SNP missense variant R/H 158 91 0.09 449 possibly damaging 0.448 23001 likely benign 23
474 TP53 rs587780068 SNP missense variant R/C 158 1 0 1000 probably damaging 0.999 25001 likely benign 25
475 TP53 rs1131691023 SNP missense variant V/A 157 1 0 927 probably damaging 0.926 25001 likely benign 25
476 TP53 rs1131691023 SNP missense variant V/D 157 1 0 999 probably damaging 0.998 25001 likely benign 25
477 TP53 rs121912654 SNP missense variant V/F 157 1 0 984 probably damaging 0.983 22001 likely benign 22
478 TP53 rs121912654 SNP missense variant V/I 157 751 0.75 42 benign 0.041 15001 likely benign 15
479 TP53 rs371524413 SNP missense variant R/P 156 121 0.12 859 possibly damaging 0.858 22001 likely benign 22
480 TP53 rs371524413 SNP missense variant R/H 156 261 0.26 21 benign 0.02 20001 likely benign 20
481 TP53 rs563378859 SNP missense variant R/C 156 231 0.23 19 benign 0.018 17001 likely benign 17
482 TP53 rs786202752 SNP missense variant T/S 155 701 0.7 7 benign 0.006 4001 likely benign 4
483 TP53 rs786202752 SNP missense variant T/N 155 1 0 616 possibly damaging 0.615 14001 likely benign 14
484 TP53 rs772683278 SNP missense variant T/A 155 921 0.92 4 benign 0.003 5001 likely benign 5
485 TP53 rs762846821 SNP missense variant G/V 154 1 0 980 probably damaging 0.979 22001 likely benign 22
486 TP53 rs762846821 SNP missense variant G/D 154 31 0.03 283 benign 0.282 17001 likely benign 17
487 TP53 rs137852789 SNP missense variant G/R 154 1 0 986 probably damaging 0.985 22001 likely benign 22
488 TP53 rs137852789 SNP missense variant G/S 154 101 0.1 309 benign 0.308 18001 likely benign 18
489 TP53 rs1064795860 SNP missense variant P/S 153 51 0.05 326 benign 0.325 7001 likely benign 7
490 TP53 rs587782705 SNP missense variant P/L 152 41 0.04 820 possibly damaging 0.819 24001 likely benign 24
491 TP53 rs767328513 SNP missense variant P/S 152 1 0 990 probably damaging 0.989 25001 likely benign 25
492 TP53 rs1057520000 SNP missense variant P/R 151 1 0 998 probably damaging 0.997 25001 likely benign 25
493 TP53 rs1057520000 SNP missense variant P/H 151 1 0 942 probably damaging 0.941 25001 likely benign 25
494 TP53 rs28934874 SNP missense variant P/S 151 11 0.01 892 possibly damaging 0.891 25001 likely benign 25
495 TP53 rs28934874 SNP missense variant P/A 151 11 0.01 922 probably damaging 0.921 24001 likely benign 24
496 TP53 rs28934874 SNP missense variant P/T 151 1 0 892 possibly damaging 0.891 24001 likely benign 24
497 TP53 rs1555526214 SNP missense variant S/F 149 91 0.09 101 benign 0.1 19001 likely benign 19
498 TP53 rs1046611742 SNP missense variant D/A 148 321 0.32 1 benign 0 3001 likely benign 3
499 TP53 rs1131691007 SNP missense variant D/Y 148 11 0.01 605 possibly damaging 0.604 21001 likely benign 21
500 TP53 rs1131691007 SNP missense variant D/N 148 351 0.35 1 benign 0 10001 likely benign 10
501 TP53 rs1453167097 SNP missense variant V/G 147 1 0 931 probably damaging 0.93 25001 likely benign 25
502 TP53 rs1555526226 SNP missense variant V/I 147 11 0.01 79 benign 0.078 19001 likely benign 19
503 TP53 rs786203064 SNP missense variant W/G 146 341 0.34 341 benign 0.34 19001 likely benign 19
504 TP53 rs587782197 SNP missense variant L/P 145 61 0.06 159 benign 0.158 23001 likely benign 23
505 TP53 rs587782197 SNP missense variant L/Q 145 1 0 866 possibly damaging 0.865 26001 likely benign 26
506 TP53 rs786201419 SNP missense variant Q/H 144 21 0.02 802 possibly damaging 0.801 23001 likely benign 23
507 TP53 rs786203071 SNP missense variant Q/L 144 81 0.08 469 possibly damaging 0.468 23001 likely benign 23
508 TP53 rs786203071 SNP missense variant Q/P 144 1 0 996 probably damaging 0.995 25001 likely benign 25
509 TP53 rs1555526241 SNP missense variant V/G 143 1 0 1000 probably damaging 0.999 26001 likely benign 26
510 TP53 rs587782620 SNP missense variant V/L 143 51 0.05 890 possibly damaging 0.889 22001 likely benign 22
511 TP53 rs587782620 SNP missense variant V/M 143 1 0 998 probably damaging 0.997 24001 likely benign 24
512 TP53 rs779196500 SNP missense variant P/L 142 21 0.02 997 probably damaging 0.996 28001 likely benign 28
513 TP53 rs1057519977 SNP missense variant C/W 141 1 0 1000 probably damaging 0.999 24001 likely benign 24
514 TP53 rs587781288 SNP missense variant C/F 141 1 0 991 probably damaging 0.99 26001 likely benign 26
515 TP53 rs587781288 SNP missense variant C/Y 141 1 0 867 possibly damaging 0.866 27001 likely benign 27
516 TP53 rs1057519978 SNP missense variant C/G 141 1 0 1001 probably damaging 1 27001 likely benign 27
517 TP53 rs1057519978 SNP missense variant C/R 141 1 0 1001 probably damaging 1 28001 likely benign 28
518 TP53 rs1057519978 SNP missense variant C/S 141 111 0.11 1000 probably damaging 0.999 24001 likely benign 24
519 TP53 rs786202561 SNP missense variant T/N 140 1 0 880 possibly damaging 0.879 26001 likely benign 26
520 TP53 rs1567554121 SNP missense variant K/N 139 11 0.01 853 possibly damaging 0.852 23001 likely benign 23
521 TP53 rs1212996409 SNP missense variant K/E 139 1 0 972 probably damaging 0.971 28001 likely benign 28
522 TP53 rs750600586 SNP missense variant A/V 138 21 0.02 981 probably damaging 0.98 25001 likely benign 25
523 TP53 rs750600586 SNP missense variant A/D 138 1 0 988 probably damaging 0.987 26001 likely benign 26
524 TP53 rs28934875 SNP missense variant A/P 138 1 0 995 probably damaging 0.994 28001 likely benign 28
525 TP53 rs758781593 SNP missense variant Q/H 136 1 0 992 probably damaging 0.991 23001 likely benign 23
526 TP53 rs758781593 SNP missense variant Q/H 136 1 0 992 probably damaging 0.991 23001 likely benign 23
527 TP53 rs1567554216 SNP missense variant Q/P 136 1 0 997 probably damaging 0.996 28001 likely benign 28
528 TP53 rs1555526268 SNP missense variant Q/E 136 1 0 945 probably damaging 0.944 26001 likely benign 26
529 TP53 rs1057519976 SNP missense variant C/W 135 1 0 1001 probably damaging 1 25001 likely benign 25
530 TP53 rs587781991 SNP missense variant C/F 135 1 0 1001 probably damaging 1 27001 likely benign 27
531 TP53 rs587781991 SNP missense variant C/Y 135 1 0 1001 probably damaging 1 28001 likely benign 28
532 TP53 rs1057519975 SNP missense variant C/G 135 11 0.01 1001 probably damaging 1 29001 likely benign 29
533 TP53 rs1057519975 SNP missense variant C/R 135 1 0 1001 probably damaging 1 29001 likely benign 29
534 TP53 rs1057519975 SNP missense variant C/S 135 1 0 1001 probably damaging 1 31001 likely deleterious 31
535 TP53 rs780442292 SNP missense variant F/C 134 1 0 1001 probably damaging 1 28001 likely benign 28
536 TP53 rs267605077 SNP missense variant F/L 134 1 0 994 probably damaging 0.993 29001 likely benign 29
537 TP53 rs267605077 SNP missense variant F/I 134 1 0 999 probably damaging 0.998 29001 likely benign 29
538 TP53 rs1064795139 SNP missense variant M/I 133 1 0 8 benign 0.007 18001 likely benign 18
539 TP53 rs28934873 SNP missense variant M/T 133 1 0 125 benign 0.124 23001 likely benign 23
540 TP53 rs1057280220 SNP missense variant M/V 133 11 0.01 4 benign 0.003 21001 likely benign 21
541 TP53 rs866775781 SNP missense variant K/N 132 11 0.01 999 probably damaging 0.998 25001 likely benign 25
542 TP53 rs866775781 SNP missense variant K/N 132 11 0.01 999 probably damaging 0.998 25001 likely benign 25
543 TP53 rs1057519996 SNP missense variant K/M 132 41 0.04 844 possibly damaging 0.843 28001 likely benign 28
544 TP53 rs1057519996 SNP missense variant K/R 132 1 0 989 probably damaging 0.988 33001 likely deleterious 33
545 TP53 rs1057519996 SNP missense variant K/T 132 1 0 996 probably damaging 0.995 32001 likely deleterious 32
546 TP53 rs747342068 SNP missense variant K/E 132 1 0 990 probably damaging 0.989 31001 likely deleterious 31
547 TP53 rs747342068 SNP missense variant K/Q 132 1 0 980 probably damaging 0.979 28001 likely benign 28
548 TP53 rs769270327 SNP missense variant N/K 131 411 0.41 999 probably damaging 0.998 24001 likely benign 24
549 TP53 rs1131691037 SNP missense variant N/I 131 1 0 999 probably damaging 0.998 28001 likely benign 28
550 TP53 rs587782160 SNP missense variant N/Y 131 1 0 1000 probably damaging 0.999 27001 likely benign 27
551 TP53 rs1131691013 SNP missense variant L/P 130 1 0 1001 probably damaging 1 29001 likely benign 29
552 TP53 rs863224683 SNP missense variant L/F 130 1 0 1001 probably damaging 1 26001 likely benign 26
553 TP53 rs863224683 SNP missense variant L/V 130 51 0.05 999 probably damaging 0.998 25001 likely benign 25
554 TP53 rs137852792 SNP missense variant A/V 129 291 0.29 1 benign 0 1 likely benign 0
555 TP53 rs137852792 SNP missense variant A/G 129 381 0.38 1 benign 0 1 likely benign 0
556 TP53 rs1438095083 SNP missense variant A/T 129 571 0.57 1 benign 0 1 likely benign 0
557 TP53 rs1555526327 SNP missense variant P/T 128 181 0.18 199 benign 0.198 16001 likely benign 16
558 TP53 rs730881999 SNP missense variant S/F 127 1 0 1001 probably damaging 1 27001 likely benign 27
559 TP53 rs730881999 SNP missense variant S/C 127 1 0 1001 probably damaging 1 27001 likely benign 27
560 TP53 rs1555526335 SNP missense variant Y/C 126 1 0 1001 probably damaging 1 32001 likely deleterious 32
561 TP53 rs886039483 SNP missense variant Y/D 126 1 0 1000 probably damaging 0.999 32001 likely deleterious 32
562 TP53 rs886039483 SNP missense variant Y/N 126 1 0 1000 probably damaging 0.999 32001 likely deleterious 32
563 TP53 rs786201057 SNP missense variant T/M 125 41 0.04 976 probably damaging 0.975 32001 likely deleterious 32
564 TP53 rs786201057 SNP missense variant T/R 125 1 0 1000 probably damaging 0.999 32001 likely deleterious 32
565 TP53 rs786201057 SNP missense variant T/K 125 1 0 997 probably damaging 0.996 31001 likely deleterious 31
566 TP53 rs1057520003 SNP missense variant T/P 125 1 0 999 probably damaging 0.998 31001 likely deleterious 31
567 TP53 rs730881997 SNP missense variant C/G 124 81 0.08 974 probably damaging 0.973 24001 likely benign 24
568 TP53 rs730881997 SNP missense variant C/S 124 491 0.49 708 possibly damaging 0.707 18001 likely benign 18
569 TP53 rs1555526486 SNP missense variant T/I 123 11 0.01 930 probably damaging 0.929 24001 likely benign 24
570 TP53 rs587781495 SNP missense variant V/M 122 1 0 994 probably damaging 0.993 23001 likely benign 23
571 TP53 rs121912658 SNP missense variant K/E 120 11 0.01 1000 probably damaging 0.999 27001 likely benign 27
572 TP53 rs121912658 SNP missense variant K/Q 120 1 0 1000 probably damaging 0.999 26001 likely benign 26
573 TP53 rs1555526506 SNP missense variant A/P 119 1 0 999 probably damaging 0.998 25001 likely benign 25
574 TP53 rs1064794141 SNP missense variant T/I 118 11 0.01 1000 probably damaging 0.999 25001 likely benign 25
575 TP53 rs755238756 SNP missense variant G/A 117 11 0.01 981 probably damaging 0.98 24001 likely benign 24
576 TP53 rs755238756 SNP missense variant G/E 117 41 0.04 999 probably damaging 0.998 25001 likely benign 25
577 TP53 rs1555526518 SNP missense variant G/R 117 1 0 1000 probably damaging 0.999 25001 likely benign 25
578 TP53 rs989692988 SNP missense variant S/A 116 31 0.03 821 possibly damaging 0.82 25001 likely benign 25
579 TP53 rs730881996 SNP missense variant H/R 115 31 0.03 6 benign 0.005 20001 likely benign 20
580 TP53 rs1555526532 SNP missense variant H/N 115 81 0.08 8 benign 0.007 14001 likely benign 14
581 TP53 rs1567555626 SNP missense variant L/F 114 71 0.07 629 possibly damaging 0.628 22001 likely benign 22
582 TP53 rs781724995 SNP missense variant L/S 114 531 0.53 775 possibly damaging 0.774 24001 likely benign 24
583 TP53 rs1567555667 SNP missense variant F/C 113 1 0 1001 probably damaging 1 28001 likely benign 28
584 TP53 rs587781642 SNP missense variant F/V 113 1 0 1001 probably damaging 1 27001 likely benign 27
585 TP53 rs1390502714 SNP missense variant G/A 112 611 0.61 34 benign 0.033 17001 likely benign 17
586 TP53 rs1423803759 SNP missense variant G/S 112 801 0.8 451 possibly damaging 0.45 21001 likely benign 21
587 TP53 rs1057519997 SNP missense variant L/R 111 1 0 995 probably damaging 0.994 25001 likely benign 25
588 TP53 rs1057519997 SNP missense variant L/P 111 1 0 999 probably damaging 0.998 26001 likely benign 26
589 TP53 rs1057519997 SNP missense variant L/Q 111 1 0 997 probably damaging 0.996 25001 likely benign 25
590 TP53 rs11540654 SNP missense variant R/L 110 51 0.05 298 benign 0.297 17001 likely benign 17
591 TP53 rs11540654 SNP missense variant R/P 110 41 0.04 808 possibly damaging 0.807 22001 likely benign 22
592 TP53 rs11540654 SNP missense variant R/H 110 171 0.17 10 benign 0.009 13001 likely benign 13
593 TP53 rs587781371 SNP missense variant R/C 110 161 0.16 46 benign 0.045 21001 likely benign 21
594 TP53 rs587781371 SNP missense variant R/S 110 121 0.12 405 benign 0.404 23001 likely benign 23
595 TP53 rs1064796722 SNP missense variant F/C 109 1 0 1001 probably damaging 1 29001 likely benign 29
596 TP53 rs1064796722 SNP missense variant F/S 109 1 0 1001 probably damaging 1 31001 likely deleterious 31
597 TP53 rs1057523496 SNP missense variant F/V 109 1 0 1001 probably damaging 1 26001 likely benign 26
598 TP53 rs587782461 SNP missense variant G/C 108 1 0 494 possibly damaging 0.493 23001 likely benign 23
599 TP53 rs587782461 SNP missense variant G/R 108 101 0.1 301 benign 0.3 20001 likely benign 20
600 TP53 rs587782461 SNP missense variant G/S 108 151 0.15 326 benign 0.325 22001 likely benign 22
601 TP53 rs587782447 SNP missense variant Y/C 107 71 0.07 233 benign 0.232 22001 likely benign 22
602 TP53 rs587782447 SNP missense variant Y/S 107 41 0.04 493 possibly damaging 0.492 24001 likely benign 24
603 TP53 rs368771578 SNP missense variant Y/H 107 711 0.71 114 benign 0.113 22001 likely benign 22
604 TP53 rs368771578 SNP missense variant Y/N 107 11 0.01 926 probably damaging 0.925 25001 likely benign 25
605 TP53 rs1555526581 SNP missense variant S/R 106 211 0.21 6 benign 0.005 6001 likely benign 6
606 TP53 rs1567555883 SNP missense variant S/I 106 71 0.07 58 benign 0.057 1001 likely benign 1
607 TP53 rs587781504 SNP missense variant G/V 105 1 0 998 probably damaging 0.997 27001 likely benign 27
608 TP53 rs587781504 SNP missense variant G/D 105 1 0 995 probably damaging 0.994 24001 likely benign 24
609 TP53 rs1060501195 SNP missense variant G/R 105 1 0 998 probably damaging 0.997 24001 likely benign 24
610 TP53 rs1060501195 SNP missense variant G/S 105 51 0.05 902 possibly damaging 0.901 23001 likely benign 23
611 TP53 rs1555526589 SNP missense variant Y/H 103 21 0.02 994 probably damaging 0.993 26001 likely benign 26
612 TP53 rs786202717 SNP missense variant T/I 102 11 0.01 45 benign 0.044 23001 likely benign 23
613 TP53 rs1567555968 SNP missense variant T/S 102 31 0.03 84 benign 0.083 17001 likely benign 17
614 TP53 rs878854069 SNP missense variant K/N 101 131 0.13 38 benign 0.037 17001 likely benign 17
615 TP53 rs1373046761 SNP missense variant K/E 101 461 0.46 19 benign 0.018 19001 likely benign 19
616 TP53 rs1567556019 SNP missense variant S/F 99 1 0 969 probably damaging 0.968 25001 likely benign 25
617 TP53 rs1567556019 SNP missense variant S/C 99 11 0.01 150 benign 0.149 24001 likely benign 24
618 TP53 rs1245723119 SNP missense variant P/L 98 1 0 1001 probably damaging 1 28001 likely benign 28
619 TP53 rs730881995 SNP missense variant V/D 97 1 0 997 probably damaging 0.996 28001 likely benign 28
620 TP53 rs730882023 SNP missense variant V/F 97 21 0.02 997 probably damaging 0.996 25001 likely benign 25
621 TP53 rs730882023 SNP missense variant V/L 97 31 0.03 800 possibly damaging 0.799 24001 likely benign 24
622 TP53 rs730882023 SNP missense variant V/I 97 421 0.42 608 possibly damaging 0.607 24001 likely benign 24
623 TP53 rs1210700121 SNP missense variant P/L 92 1 0 336 benign 0.335 23001 likely benign 23
624 TP53 rs1555526625 SNP missense variant S/F 90 141 0.14 731 possibly damaging 0.73 17001 likely benign 17
625 TP53 rs730881994 SNP missense variant P/L 89 161 0.16 95 benign 0.094 14001 likely benign 14
626 TP53 rs1555526631 SNP missense variant A/V 88 391 0.39 31 benign 0.03 12001 likely benign 12
627 TP53 rs1567556231 SNP missense variant A/P 88 281 0.28 19 benign 0.018 12001 likely benign 12
628 TP53 rs587782148 SNP missense variant A/T 86 501 0.5 12 benign 0.011 1 likely benign 0
629 TP53 rs587781307 SNP missense variant A/T 84 461 0.46 13 benign 0.012 4001 likely benign 4
630 TP53 rs201717599 SNP missense variant A/V 83 251 0.25 8 benign 0.007 1 likely benign 0
631 TP53 rs201717599 SNP missense variant A/E 83 721 0.72 39 benign 0.038 1 likely benign 0
632 TP53 rs534447939 SNP missense variant P/L 82 101 0.1 8 benign 0.007 3001 likely benign 3
633 TP53 rs534447939 SNP missense variant P/R 82 71 0.07 512 possibly damaging 0.511 4001 likely benign 4
634 TP53 rs1555526664 SNP missense variant P/A 82 331 0.33 8 benign 0.007 4001 likely benign 4
635 TP53 rs1567556386 SNP missense variant T/I 81 261 0.26 2 benign 0.001 3001 likely benign 3
636 TP53 rs1060501204 SNP missense variant P/S 80 261 0.26 51 benign 0.05 7001 likely benign 7
637 TP53 rs876658527 SNP missense variant A/G 78 241 0.24 288 benign 0.287 3001 likely benign 3
638 TP53 rs1555526673 SNP missense variant A/T 78 441 0.44 21 benign 0.02 2001 likely benign 2
639 TP53 rs753085009 SNP missense variant P/S 77 491 0.49 74 benign 0.073 1 likely benign 0
640 TP53 rs753085009 SNP missense variant P/T 77 211 0.21 31 benign 0.03 1 likely benign 0
641 TP53 rs1235781676 SNP missense variant A/E 76 781 0.78 35 benign 0.034 1 likely benign 0
642 TP53 rs587781832 SNP missense variant A/V 74 281 0.28 372 benign 0.371 1 likely benign 0
643 TP53 rs587782423 SNP missense variant V/M 73 231 0.23 14 benign 0.013 1 likely benign 0
644 TP53 rs878854066 substitution missense variant P/R 72 361 0.36 355 benign 0.354 5001 likely benign 5
645 TP53 rs730882014 substitution missense variant P/C 72 151 0.15 616 possibly damaging 0.615 -
646 TP53 rs1042522 SNP missense variant P/R 72 361 0.36 355 benign 0.354 5001 likely benign 5
647 TP53 rs1042522 SNP missense variant P/H 72 511 0.51 453 possibly damaging 0.452 7001 likely benign 7
648 TP53 rs587782769 SNP missense variant P/S 72 701 0.7 7 benign 0.006 1 likely benign 0
649 TP53 rs587782769 SNP missense variant P/A 72 661 0.66 2 benign 0.001 1 likely benign 0
650 TP53 rs587782769 SNP missense variant P/T 72 421 0.42 4 benign 0.003 1 likely benign 0
651 TP53 rs878854065 SNP missense variant P/R 71 151 0.15 112 benign 0.111 4001 likely benign 4
652 TP53 rs1567556576 SNP missense variant P/S 71 621 0.62 13 benign 0.012 1 likely benign 0
653 TP53 rs1567556576 SNP missense variant P/A 71 701 0.7 2 benign 0.001 1 likely benign 0
654 TP53 rs1567556594 SNP missense variant A/V 70 251 0.25 97 benign 0.096 9001 likely benign 9
655 TP53 rs756233241 SNP missense variant A/V 69 391 0.39 30 benign 0.029 7001 likely benign 7
656 TP53 rs756233241 SNP missense variant A/G 69 441 0.44 21 benign 0.02 4001 likely benign 4
657 TP53 rs1567556618 SNP missense variant A/T 69 601 0.6 21 benign 0.02 1 likely benign 0
658 TP53 rs869312782 SNP missense variant E/Q 68 451 0.45 42 benign 0.041 3001 likely benign 3
659 TP53 rs1555526709 SNP missense variant P/Q 67 241 0.24 15 benign 0.014 3001 likely benign 3
660 TP53 rs1555526711 SNP missense variant M/I 66 201 0.2 4 benign 0.003 1 likely benign 0
661 TP53 rs1060501210 SNP missense variant R/T 65 581 0.58 4 benign 0.003 1 likely benign 0
662 TP53 rs372201428 SNP missense variant A/V 63 241 0.24 13 benign 0.012 4001 likely benign 4
663 TP53 rs372201428 SNP missense variant A/G 63 191 0.19 13 benign 0.012 6001 likely benign 6
664 TP53 rs876658902 SNP missense variant A/T 63 271 0.27 8 benign 0.007 3001 likely benign 3
665 TP53 rs1460793472 SNP missense variant D/G 61 141 0.14 13 benign 0.012 15001 likely benign 15
666 TP53 rs1237722021 SNP missense variant G/C 59 81 0.08 167 benign 0.166 6001 likely benign 6
667 TP53 rs144386518 SNP missense variant P/R 58 481 0.48 905 possibly damaging 0.904 1001 likely benign 1
668 TP53 rs587782776 SNP missense variant D/E 57 541 0.54 6 benign 0.005 1 likely benign 0
669 TP53 rs1442824382 SNP missense variant D/G 57 271 0.27 2 benign 0.001 1 likely benign 0
670 TP53 rs1555526742 SNP missense variant F/L 54 1001 1 1 benign 0 1 likely benign 0
671 TP53 rs774656101 SNP missense variant Q/R 52 431 0.43 8 benign 0.007 2001 likely benign 2
672 TP53 rs1567556923 SNP missense variant E/G 51 261 0.26 63 benign 0.062 1 likely benign 0
673 TP53 rs370502517 SNP missense variant I/T 50 451 0.45 8 benign 0.007 5001 likely benign 5
674 TP53 rs370502517 SNP missense variant I/N 50 251 0.25 99 benign 0.098 9001 likely benign 9
675 TP53 rs759728549 SNP missense variant D/G 49 161 0.16 42 benign 0.041 6001 likely benign 6
676 TP53 rs587780728 SNP missense variant D/H 49 31 0.03 914 probably damaging 0.913 16001 likely benign 16
677 TP53 rs587780728 SNP missense variant D/N 49 201 0.2 63 benign 0.062 5001 likely benign 5
678 TP53 rs587781460 SNP missense variant D/E 48 1001 1 4 benign 0.003 1 likely benign 0
679 TP53 rs1800371 SNP missense variant P/S 47 201 0.2 21 benign 0.02 1 likely benign 0
680 TP53 rs1800371 SNP missense variant P/T 47 201 0.2 13 benign 0.012 1 likely benign 0
681 TP53 rs876659630 SNP missense variant S/P 46 241 0.24 2 benign 0.001 5001 likely benign 5
682 TP53 rs879254066 SNP missense variant L/P 45 21 0.02 21 benign 0.02 15001 likely benign 15
683 TP53 rs1060501190 SNP missense variant M/I 44 241 0.24 6 benign 0.005 1 likely benign 0
684 TP53 rs754332870 SNP missense variant L/F 43 161 0.16 223 benign 0.222 12001 likely benign 12
685 TP53 rs587781767 SNP missense variant D/G 42 111 0.11 30 benign 0.029 14001 likely benign 14
686 TP53 rs756847009 SNP missense variant D/N 42 191 0.19 21 benign 0.02 10001 likely benign 10
687 TP53 rs1555526789 SNP missense variant D/N 41 261 0.26 21 benign 0.02 9001 likely benign 9
688 TP53 rs587782877 SNP missense variant M/T 40 361 0.36 63 benign 0.062 4001 likely benign 4
689 TP53 rs1353016807 SNP missense variant A/V 39 151 0.15 140 benign 0.139 5001 likely benign 5
690 TP53 rs1567557177 SNP missense variant S/F 37 11 0.01 558 possibly damaging 0.557 15001 likely benign 15
691 TP53 rs587781866 SNP missense variant P/L 36 401 0.4 1 benign 0 1001 likely benign 1
692 TP53 rs587781866 SNP missense variant P/Q 36 591 0.59 193 benign 0.192 1 likely benign 0
693 TP53 rs730881993 SNP missense variant P/S 36 761 0.76 27 benign 0.026 1 likely benign 0
694 TP53 rs121912661 SNP missense variant L/F 35 731 0.73 214 benign 0.213 1 likely benign 0
695 TP53 rs121912661 SNP missense variant L/F 35 731 0.73 214 benign 0.213 1 likely benign 0
696 TP53 rs1060501211 SNP missense variant L/M 35 231 0.23 310 benign 0.309 5001 likely benign 5
697 TP53 rs1322947350 SNP missense variant P/R 34 91 0.09 92 benign 0.091 7001 likely benign 7
698 TP53 rs786201968 SNP missense variant P/A 34 201 0.2 4 benign 0.003 1 likely benign 0
699 TP53 rs786201968 SNP missense variant P/T 34 251 0.25 1 benign 0 1 likely benign 0
700 TP53 rs1555526832 SNP missense variant S/Y 33 231 0.23 30 benign 0.029 10001 likely benign 10
701 TP53 rs201753350 SNP missense variant V/F 31 161 0.16 23 benign 0.022 12001 likely benign 12
702 TP53 rs201753350 SNP missense variant V/I 31 261 0.26 6 benign 0.005 8001 likely benign 8
703 TP53 rs1011445550 SNP missense variant N/K 29 771 0.77 2 benign 0.001 8001 likely benign 8
704 TP53 rs786202289 SNP missense variant E/V 28 201 0.2 288 benign 0.287 22001 likely benign 22
705 TP53 rs1555526933 SNP missense variant P/L 27 81 0.08 161 benign 0.16 23001 likely benign 23
706 TP53 rs922736614 SNP missense variant P/S 27 111 0.11 273 benign 0.272 23001 likely benign 23
707 TP53 rs922736614 SNP missense variant P/T 27 151 0.15 250 benign 0.249 25001 likely benign 25
708 TP53 rs1800369 SNP missense variant D/E 21 531 0.53 18 benign 0.017 13001 likely benign 13
709 TP53 rs876659913 SNP missense variant S/P 20 111 0.11 133 benign 0.132 22001 likely benign 22
710 TP53 rs1567558112 SNP missense variant L/V 14 51 0.05 768 possibly damaging 0.767 23001 likely benign 23
711 TP53 rs878854070 SNP missense variant P/L 13 1 0 623 possibly damaging 0.622 25001 likely benign 25
712 TP53 rs878854070 SNP missense variant P/R 13 1 0 989 probably damaging 0.988 24001 likely benign 24
713 TP53 rs1060501208 SNP missense variant P/S 13 51 0.05 741 possibly damaging 0.74 23001 likely benign 23
714 TP53 rs1482497533 SNP missense variant P/L 12 521 0.52 25 benign 0.024 11001 likely benign 11
715 TP53 rs1482497533 SNP missense variant P/R 12 191 0.19 852 possibly damaging 0.851 18001 likely benign 18
716 TP53 rs1482497533 SNP missense variant P/H 12 71 0.07 941 probably damaging 0.94 22001 likely benign 22
717 TP53 rs201382018 SNP missense variant E/Q 11 41 0.04 952 probably damaging 0.951 23001 likely benign 23
718 TP53 rs201382018 SNP missense variant E/K 11 11 0.01 892 possibly damaging 0.891 23001 likely benign 23
719 TP53 rs1418778734 SNP missense variant V/G 10 71 0.07 188 benign 0.187 13001 likely benign 13
720 TP53 rs535274413 SNP missense variant V/L 10 1001 1 4 benign 0.003 1 likely benign 0
721 TP53 rs535274413 SNP missense variant V/I 10 551 0.55 2 benign 0.001 1 likely benign 0
722 TP53 rs757282628 SNP missense variant S/R 9 231 0.23 711 possibly damaging 0.71 9001 likely benign 9
723 TP53 rs1555527015 SNP missense variant S/N 9 251 0.25 13 benign 0.012 1 likely benign 0
724 TP53 rs1555527017 SNP missense variant S/R 9 231 0.23 711 possibly damaging 0.71 9001 likely benign 9
725 TP53 rs876659415 SNP missense variant P/L 8 421 0.42 1 benign 0 4001 likely benign 4
726 TP53 rs587781277 SNP missense variant D/E 7 381 0.38 95 benign 0.094 1 likely benign 0
727 TP53 rs587781277 SNP missense variant D/E 7 381 0.38 95 benign 0.094 1 likely benign 0
728 TP53 rs587782646 SNP missense variant D/H 7 1 0 979 probably damaging 0.978 23001 likely benign 23
729 TP53 rs1357147493 SNP missense variant S/P 6 61 0.06 852 possibly damaging 0.851 15001 likely benign 15
730 TP53 rs781595324 SNP missense variant Q/R 5 161 0.16 140 benign 0.139 7001 likely benign 7
731 TP53 rs878854064 SNP missense variant P/L 4 41 0.04 32 benign 0.031 9001 likely benign 9
732 TP53 rs878854064 SNP missense variant P/R 4 11 0.01 799 possibly damaging 0.798 14001 likely benign 14
733 TP53 rs1356004172 SNP missense variant P/T 4 51 0.05 45 benign 0.044 1 likely benign 0
734 TP53 rs786203938 SNP missense variant E/G 3 1 0 778 possibly damaging 0.777 24001 likely benign 24
735 TP53 rs769884991 SNP missense variant E/K 2 11 0.01 842 possibly damaging 0.841 23001 likely benign 23
736 PIK3CA rs751557352 SNP missense variant S/T 2 11 0.01 842 possibly damaging 0.841 20001 likely benign 20
737 PIK3CA rs1220116506 SNP missense variant R/Q 3 21 0.02 975 probably damaging 0.974 23001 likely benign 23
738 PIK3CA rs1260684206 SNP missense variant E/G 4 1 0 1001 probably damaging 1 24001 likely benign 24
739 PIK3CA rs1436163100 SNP missense variant G/E 6 1 0 1001 probably damaging 1 22001 likely benign 22
740 PIK3CA rs369950390 SNP missense variant Y/C 9 171 0.17 86 benign 0.085 23001 likely benign 23
741 PIK3CA rs199747934 SNP missense variant H/N 11 221 0.22 8 benign 0.007 20001 likely benign 20
742 PIK3CA rs201631515 SNP missense variant A/T 12 951 0.95 4 benign 0.003 20001 likely benign 20
743 PIK3CA rs201631515 SNP missense variant A/S 12 791 0.79 4 benign 0.003 18001 likely benign 18
744 PIK3CA rs200031978 SNP missense variant G/V 13 101 0.1 418 benign 0.417 21001 likely benign 21
745 PIK3CA rs201371389 SNP missense variant N/S 16 481 0.48 10 benign 0.009 19001 likely benign 19
746 PIK3CA rs1423200481 SNP missense variant L/F 24 11 0.01 860 possibly damaging 0.859 20001 likely benign 20
747 PIK3CA rs104885999 SNP missense variant R/K 25 141 0.14 139 benign 0.138 19001 likely benign 19
748 PIK3CA rs1302938521 SNP missense variant D/G 28 11 0.01 991 probably damaging 0.99 27001 likely benign 27
749 PIK3CA rs59971989 SNP missense variant K/E 29 911 0.91 186 benign 0.185 19001 likely benign 19
750 PIK3CA rs1387024511 SNP missense variant K/Q 33 21 0.02 140 benign 0.139 16001 likely benign 16
751 PIK3CA rs1266238180 SNP missense variant K/R 33 1001 1 1 benign 0 16001 likely benign 16
752 PIK3CA rs1560144842 SNP missense variant A/T 34 241 0.24 87 benign 0.086 21001 likely benign 21
753 PIK3CA rs1466575763 SNP missense variant I/V 35 341 0.34 7 benign 0.006 17001 likely benign 17
754 PIK3CA rs121913285 SNP missense variant P/R 40 1 0 996 probably damaging 0.995 26001 likely benign 26
755 PIK3CA rs121913273 SNP missense variant E/K 43 1 0 1000 probably damaging 0.999 32001 likely deleterious 32
756 PIK3CA rs121913273 SNP missense variant E/Q 43 1 0 1000 probably damaging 0.999 25001 likely benign 25
757 PIK3CA rs1057519927 SNP missense variant E/A 43 1 0 1000 probably damaging 0.999 27001 likely benign 27
758 PIK3CA rs1057519927 SNP missense variant E/G 43 1 0 1001 probably damaging 1 23001 likely benign 23
759 PIK3CA rs1057519927 SNP missense variant E/V 43 1 0 1001 probably damaging 1 31001 likely deleterious 31
760 PIK3CA rs104886003 SNP missense variant E/K 46 1 0 1000 probably damaging 0.999 31001 likely deleterious 31
761 PIK3CA rs104886003 SNP missense variant E/Q 46 1 0 1000 probably damaging 0.999 24001 likely benign 24
762 PIK3CA rs121913274 SNP missense variant E/A 46 1 0 1000 probably damaging 0.999 27001 likely benign 27
763 PIK3CA rs121913274 SNP missense variant E/G 46 1 0 1001 probably damaging 1 31001 likely deleterious 31
764 PIK3CA rs121913274 SNP missense variant E/V 46 1 0 1001 probably damaging 1 28001 likely benign 28
765 PIK3CA rs121913275 SNP missense variant E/D 46 1 0 1000 probably damaging 0.999 23001 likely benign 23
766 PIK3CA rs121913275 SNP missense variant E/D 46 1 0 1000 probably damaging 0.999 23001 likely benign 23
767 PIK3CA rs121913286 SNP missense variant Q/K 47 1 0 1000 probably damaging 0.999 25001 likely benign 25
768 PIK3CA rs121913286 SNP missense variant Q/E 47 1 0 1000 probably damaging 0.999 21001 likely benign 21
769 PIK3CA rs397517201 SNP missense variant Q/P 47 1 0 1001 probably damaging 1 27001 likely benign 27
770 PIK3CA rs397517201 SNP missense variant Q/R 47 1 0 1000 probably damaging 0.999 26001 likely benign 26
771 PIK3CA rs397517201 SNP missense variant Q/L 47 1 0 1000 probably damaging 0.999 25001 likely benign 25
772 PIK3CA rs1057519940 SNP missense variant Q/H 47 1 0 1001 probably damaging 1 21001 likely benign 21
773 PIK3CA rs1057519699 SNP missense variant D/N 50 11 0.01 976 probably damaging 0.975 25001 likely benign 25
774 PIK3CA rs988134846 SNP missense variant L/V 52 1 0 768 possibly damaging 0.767 22001 likely benign 22
775 PIK3CA rs104886000 SNP missense variant R/K 56 1 0 1000 probably damaging 0.999 33001 likely deleterious 33
776 PIK3CA rs1302992156 SNP missense variant C/Y 57 1 0 990 probably damaging 0.989 22001 likely benign 22
777 PIK3CA rs1425149965 SNP missense variant I/T 58 1 0 951 probably damaging 0.95 5001 likely benign 5
778 MYC rs778595707 SNP missense variant D/Y 2 1 0 655 possibly damaging 0.654 31001 likely deleterious 31
779 MYC rs772459508 SNP missense variant F/L 3 1 0 1 benign 0 18001 likely benign 18
780 MYC rs747141352 SNP missense variant R/Q 5 1 0 1 benign 0 22001 likely benign 22
781 MYC rs747141352 SNP missense variant R/P 5 1 0 152 benign 0.151 20001 likely benign 20
782 MYC rs777141161 SNP missense variant V/I 6 531 0.53 1 benign 0 2001 likely benign 2
783 MYC rs759986640 SNP missense variant E/G 8 511 0.51 1 benign 0 22001 likely benign 22
784 MYC rs1381903406 SNP missense variant N/I 9 211 0.21 1 benign 0 12001 likely benign 12
785 MYC rs1319018025 SNP missense variant~splice region variant Q/H 10 131 0.13 56 benign 0.055 28001 likely benign 28
786 MYC rs139294902 SNP missense variant P/R 12 61 0.06 28 benign 0.027 21001 likely benign 21
787 MYC rs770253839 SNP missense variant A/T 14 511 0.51 1 benign 0 14001 likely benign 14
788 MYC rs775909833 SNP missense variant T/K 15 31 0.03 2 benign 0.001 23001 likely benign 23
789 MYC rs1382266165 SNP missense variant P/S 17 31 0.03 958 probably damaging 0.957 27001 likely benign 27
790 MYC rs149992096 SNP missense variant N/K 19 141 0.14 191 benign 0.19 23001 likely benign 23
791 MYC rs146505192 SNP missense variant F/L 22 1001 1 8 benign 0.007 15001 likely benign 15
792 MYC rs146505192 SNP missense variant F/V 22 111 0.11 131 benign 0.13 22001 likely benign 22
793 MYC rs1490644442 SNP missense variant N/Y 24 291 0.29 801 possibly damaging 0.8 24001 likely benign 24
794 MYC rs148915481 SNP missense variant N/S 24 1001 1 8 benign 0.007 11001 likely benign 11
795 MYC rs4645959 SNP missense variant N/T 26 31 0.03 16 benign 0.015 28001 likely benign 28
796 MYC rs4645959 SNP missense variant N/S 26 11 0.01 161 benign 0.16 26001 likely benign 26
797 MYC rs1418866533 SNP missense variant Y/N 27 111 0.11 949 probably damaging 0.948 25001 likely benign 25
798 MYC rs1183060749 SNP missense variant D/V 28 1 0 1000 probably damaging 0.999 32001 likely deleterious 32
799 MYC rs375812644 SNP missense variant L/V 29 41 0.04 364 benign 0.363 25001 likely benign 25
800 MYC rs764006760 SNP missense variant Y/C 31 1 0 995 probably damaging 0.994 31001 likely deleterious 31
801 MYC rs776780683 SNP missense variant S/L 33 31 0.03 991 probably damaging 0.99 28001 likely benign 28
802 MYC rs781313941 SNP missense variant V/M 34 141 0.14 296 benign 0.295 21001 likely benign 21
803 MYC rs1395774855 SNP missense variant D/G 41 1 0 486 possibly damaging 0.485 32001 likely deleterious 32
804 MYC rs1563757581 SNP missense variant D/E 41 101 0.1 13 benign 0.012 22001 likely benign 22
805 MYC rs1391743516 SNP missense variant E/D 43 721 0.72 916 probably damaging 0.915 11001 likely benign 11
806 MYC rs745993896 SNP missense variant E/D 44 861 0.86 237 benign 0.236 23001 likely benign 23
807 MYC rs780361249 SNP missense variant F/S 46 41 0.04 644 possibly damaging 0.643 32001 likely deleterious 32
808 MYC rs114570780 SNP missense variant Y/H 47 1 0 956 probably damaging 0.955 31001 likely deleterious 31
809 MYC rs61752959 SNP missense variant Q/H 48 541 0.54 1 benign 0 15001 likely benign 15
810 MYC rs949318807 SNP missense variant Q/R 49 651 0.65 331 benign 0.33 22001 likely benign 22
811 MYC rs900683143 SNP missense variant Q/H 50 261 0.26 42 benign 0.041 22001 likely benign 22
812 MYC rs1270296696 SNP missense variant Q/K 52 611 0.61 75 benign 0.074 21001 likely benign 21
813 MYC rs1329377103 SNP missense variant Q/L 52 191 0.19 99 benign 0.098 23001 likely benign 23
814 MYC rs1250123425 SNP missense variant S/R 53 11 0.01 877 possibly damaging 0.876 27001 likely benign 27
815 MYC rs770534113 SNP missense variant E/K 54 501 0.5 385 benign 0.384 25001 likely benign 25
816 MYC rs770534113 SNP missense variant E/Q 54 641 0.64 158 benign 0.157 24001 likely benign 24
817 MYC rs121918684 SNP missense variant E/D 54 361 0.36 32 benign 0.031 23001 likely benign 23
818 MYC rs1240451313 SNP missense variant L/P 55 51 0.05 183 benign 0.182 26001 likely benign 26
819 MYC rs1240451313 SNP missense variant L/R 55 1 0 957 probably damaging 0.956 29001 likely benign 29
820 MYC rs1057519849 SNP missense variant P/S 57 1 0 623 possibly damaging 0.622 26001 likely benign 26
821 MYC rs1037072564 SNP missense variant P/L 57 1 0 983 probably damaging 0.982 29001 likely benign 29
822 MYC rs1057519918 SNP missense variant P/L 58 1 0 1000 probably damaging 0.999 29001 likely benign 29
823 MYC rs775522201 SNP missense variant A/V 59 31 0.03 997 probably damaging 0.996 29001 likely benign 29
824 MYC rs1437767389 SNP missense variant E/D 62 1 0 992 probably damaging 0.991 26001 likely benign 26
825 MYC rs751452834 SNP missense variant D/A 63 1 0 999 probably damaging 0.998 32001 likely deleterious 32
826 MYC rs1403660912 SNP missense variant L/M 70 1 0 1000 probably damaging 0.999 25001 likely benign 25
827 MYC rs28933407 SNP missense variant P/S 72 31 0.03 623 possibly damaging 0.622 28001 likely benign 28
828 MYC rs750664148 SNP missense variant T/P 73 31 0.03 969 probably damaging 0.968 25001 likely benign 25
829 MYC rs750664148 SNP missense variant T/A 73 21 0.02 344 benign 0.343 24001 likely benign 24
830 MYC rs756091827 SNP missense variant T/S 73 11 0.01 807 possibly damaging 0.806 24001 likely benign 24
831 MYC rs756091827 SNP missense variant T/I 73 1 0 899 possibly damaging 0.898 28001 likely benign 28
832 MYC rs121918685 SNP missense variant P/A 74 11 0.01 999 probably damaging 0.998 27001 likely benign 27
833 MYC rs1294281543 SNP missense variant P/L 74 1 0 1000 probably damaging 0.999 31001 likely deleterious 31
834 MYC rs780202654 SNP missense variant L/R 76 1 0 989 probably damaging 0.988 24001 likely benign 24
835 MYC rs1563757684 SNP missense variant S/T 77 1 0 987 probably damaging 0.986 25001 likely benign 25
836 MYC rs1057519850 SNP missense variant S/F 77 1 0 998 probably damaging 0.997 31001 likely deleterious 31
837 MYC rs931443247 SNP missense variant S/C 79 1 0 990 probably damaging 0.989 29001 likely benign 29
838 MYC rs1460265619 SNP missense variant R/C 80 21 0.02 336 benign 0.335 32001 likely deleterious 32
839 MYC rs375402667 SNP missense variant R/S 81 71 0.07 961 probably damaging 0.96 24001 likely benign 24
840 MYC rs375402667 SNP missense variant R/G 81 121 0.12 961 probably damaging 0.96 25001 likely benign 25
841 MYC rs375402667 SNP missense variant R/C 81 11 0.01 994 probably damaging 0.993 31001 likely deleterious 31
842 MYC rs1420068922 SNP missense variant R/H 81 11 0.01 485 possibly damaging 0.484 30001 likely deleterious 30
843 MYC rs1484385745 SNP missense variant L/V 84 181 0.18 970 probably damaging 0.969 21001 likely benign 21
844 MYC rs1184821004 SNP missense variant C/S 85 441 0.44 1 benign 0 22001 likely benign 22
845 MYC rs1184821004 SNP missense variant C/R 85 361 0.36 70 benign 0.069 23001 likely benign 23
846 MYC rs776077629 SNP missense variant C/F 85 701 0.7 44 benign 0.043 23001 likely benign 23
847 MYC rs745545434 SNP missense variant C/W 85 191 0.19 1 benign 0 25001 likely benign 25
848 MYC rs886556187 SNP missense variant S/L 86 191 0.19 948 probably damaging 0.947 24001 likely benign 24
849 MYC rs1371389460 SNP missense variant S/C 88 21 0.02 622 possibly damaging 0.621 26001 likely benign 26
850 MYC rs866188449 SNP missense variant V/I 90 421 0.42 4 benign 0.003 14001 likely benign 14
851 MYC rs866188449 SNP missense variant V/L 90 671 0.67 4 benign 0.003 14001 likely benign 14
852 MYC rs148228388 SNP missense variant A/E 91 71 0.07 453 possibly damaging 0.452 17001 likely benign 17
853 MYC rs1563757725 SNP missense variant T/R 93 361 0.36 1 benign 0 18001 likely benign 18
854 MYC rs764188937 SNP missense variant R/P 98 331 0.33 1 benign 0 23001 likely benign 23
855 MYC rs764188937 SNP missense variant R/L 98 521 0.52 134 benign 0.133 20001 likely benign 20
856 MYC rs1362063441 SNP missense variant G/E 99 271 0.27 4 benign 0.003 18001 likely benign 18
857 MYC rs1362063441 SNP missense variant G/A 99 211 0.21 6 benign 0.005 17001 likely benign 17
858 MYC rs979999500 SNP missense variant D/G 100 551 0.55 4 benign 0.003 19001 likely benign 19
859 MYC rs1383206618 SNP missense variant N/H 101 591 0.59 177 benign 0.176 19001 likely benign 19
860 MYC rs121918683 SNP missense variant N/T 101 431 0.43 22 benign 0.021 18001 likely benign 18
861 MYC rs767360326 SNP missense variant N/K 101 371 0.37 28 benign 0.027 14001 likely benign 14
862 MYC rs750561207 SNP missense variant D/G 102 411 0.41 1 benign 0 15001 likely benign 15
863 MYC rs868656085 SNP missense variant D/E 102 1001 1 149 benign 0.148 13001 likely benign 13
864 MYC rs1034655525 SNP missense variant G/D 103 121 0.12 849 possibly damaging 0.848 24001 likely benign 24
865 MYC rs199561469 SNP missense variant G/S 104 641 0.64 678 possibly damaging 0.677 24001 likely benign 24
866 MYC rs199561469 SNP missense variant G/R 104 231 0.23 916 probably damaging 0.915 25001 likely benign 25
867 MYC rs1314120778 SNP missense variant S/F 109 21 0.02 543 possibly damaging 0.542 27001 likely benign 27
868 MYC rs1296200537 SNP missense variant D/H 112 1 0 999 probably damaging 0.998 32001 likely deleterious 32
869 MYC rs755460825 SNP missense variant Q/K 113 211 0.21 317 benign 0.316 23001 likely benign 23
870 MYC rs753250129 SNP missense variant M/V 116 661 0.66 758 possibly damaging 0.757 23001 likely benign 23
871 MYC rs758629773 SNP missense variant M/I 116 511 0.51 758 possibly damaging 0.757 24001 likely benign 24
872 MYC rs769538164 SNP missense variant E/D 119 211 0.21 996 probably damaging 0.995 24001 likely benign 24
873 MYC rs901466364 SNP missense variant L/M 121 11 0.01 998 probably damaging 0.997 25001 likely benign 25
874 MYC rs1010887246 SNP missense variant N/K 127 31 0.03 397 benign 0.396 25001 likely benign 25
875 MYC rs1264239026 SNP missense variant Q/K 128 81 0.08 921 probably damaging 0.92 24001 likely benign 24
876 MYC rs1300804558 SNP missense variant S/R 129 11 0.01 999 probably damaging 0.998 25001 likely benign 25
877 MYC rs748874520 SNP missense variant F/C 130 1 0 983 probably damaging 0.982 32001 likely deleterious 32
878 MYC rs959964647 SNP missense variant F/L 130 101 0.1 538 possibly damaging 0.537 25001 likely benign 25
879 MYC rs1478921898 SNP missense variant D/N 135 111 0.11 978 probably damaging 0.977 26001 likely benign 26
880 MYC rs993100973 SNP missense variant D/G 135 241 0.24 551 possibly damaging 0.55 25001 likely benign 25
881 MYC rs768286545 SNP missense variant D/E 135 371 0.37 695 possibly damaging 0.694 22001 likely benign 22
882 MYC rs768286545 SNP missense variant D/E 135 371 0.37 695 possibly damaging 0.694 22001 likely benign 22
883 MYC rs1454889513 SNP missense variant D/N 136 101 0.1 596 possibly damaging 0.595 25001 likely benign 25
884 MYC rs1284270835 SNP missense variant D/E 136 551 0.55 968 probably damaging 0.967 14001 likely benign 14
885 MYC rs1284270835 SNP missense variant D/E 136 551 0.55 968 probably damaging 0.967 14001 likely benign 14
886 MYC rs374225230 SNP missense variant E/Q 137 701 0.7 645 possibly damaging 0.644 24001 likely benign 24
887 MYC rs771723282 SNP missense variant T/S 138 831 0.83 31 benign 0.03 14001 likely benign 14
888 MYC rs773098170 SNP missense variant T/S 138 831 0.83 31 benign 0.03 14001 likely benign 14
889 MYC rs773098170 SNP missense variant T/I 138 31 0.03 787 possibly damaging 0.786 22001 likely benign 22
890 MYC rs1317807344 SNP missense variant F/L 139 291 0.29 280 benign 0.279 22001 likely benign 22
891 MYC rs1405976268 SNP missense variant N/S 142 1001 1 14 benign 0.013 23001 likely benign 23
892 MYC rs1032014837 SNP missense variant I/V 145 11 0.01 816 possibly damaging 0.815 26001 likely benign 26
893 MYC rs150308400 SNP missense variant C/Y 148 1 0 1000 probably damaging 0.999 32001 likely deleterious 32
894 MYC rs753906871 SNP missense variant M/V 149 1 0 969 probably damaging 0.968 28001 likely benign 28
895 MYC rs1248173307 SNP missense variant G/S 152 101 0.1 916 probably damaging 0.915 27001 likely benign 27
896 MYC rs1468408630 SNP missense variant G/A 152 31 0.03 971 probably damaging 0.97 31001 likely deleterious 31
897 MYC rs1161084627 SNP missense variant A/S 157 71 0.07 995 probably damaging 0.994 27001 likely benign 27
898 MYC rs913059216 SNP missense variant K/R 158 31 0.03 938 probably damaging 0.937 25001 likely benign 25
899 MYC rs137906262 SNP missense variant L/I 159 11 0.01 998 probably damaging 0.997 28001 likely benign 28
900 MYC rs753094370 SNP missense variant V/A 160 1 0 976 probably damaging 0.975 32001 likely deleterious 32
901 MYC rs1324784102 SNP missense variant E/Q 162 1 0 985 probably damaging 0.984 32001 likely deleterious 32
902 MYC rs758986453 SNP missense variant E/D 162 1 0 968 probably damaging 0.967 26001 likely benign 26
903 MYC rs777980347 SNP missense variant S/F 166 21 0.02 976 probably damaging 0.975 28001 likely benign 28
904 MYC rs61755060 SNP missense variant Q/H 168 291 0.29 156 benign 0.155 24001 likely benign 24
905 MYC rs1374279390 SNP missense variant A/T 170 51 0.05 31 benign 0.03 26001 likely benign 26
906 MYC rs990645227 SNP missense variant R/L 171 21 0.02 967 probably damaging 0.966 32001 likely deleterious 32
907 MYC rs755827927 SNP missense variant K/Q 172 101 0.1 972 probably damaging 0.971 23001 likely benign 23
908 MYC rs755827927 SNP missense variant K/E 172 111 0.11 916 probably damaging 0.915 23001 likely benign 23
909 MYC rs967161771 SNP missense variant D/N 173 141 0.14 947 probably damaging 0.946 27001 likely benign 27
910 MYC rs748962740 SNP missense variant D/E 173 941 0.94 240 benign 0.239 23001 likely benign 23
911 MYC rs1291924699 SNP missense variant S/G 174 541 0.54 10 benign 0.009 19001 likely benign 19
912 MYC rs1436063286 SNP missense variant S/R 174 381 0.38 587 possibly damaging 0.586 23001 likely benign 23
913 MYC rs4645960 SNP missense variant G/S 175 381 0.38 2 benign 0.001 11001 likely benign 11
914 MYC rs4645960 SNP missense variant G/R 175 111 0.11 270 benign 0.269 17001 likely benign 17
915 MYC rs4645960 SNP missense variant G/C 175 181 0.18 49 benign 0.048 19001 likely benign 19
916 MYC rs1458778798 SNP missense variant P/T 177 361 0.36 16 benign 0.015 19001 likely benign 19
917 MYC rs1458778798 SNP missense variant P/A 177 1001 1 8 benign 0.007 15001 likely benign 15
918 MYC rs1384004800 SNP missense variant N/K 178 681 0.68 27 benign 0.026 15001 likely benign 15
919 MYC rs1439970381 SNP missense variant P/S 179 591 0.59 921 probably damaging 0.92 18001 likely benign 18
920 MYC rs1164555124 SNP missense variant A/S 180 311 0.31 136 benign 0.135 18001 likely benign 18
921 MYC rs1416564094 SNP missense variant A/V 180 81 0.08 601 possibly damaging 0.6 21001 likely benign 21
922 MYC rs772094171 SNP missense variant R/G 181 411 0.41 4 benign 0.003 22001 likely benign 22
923 MYC rs772094171 SNP missense variant R/C 181 61 0.06 782 possibly damaging 0.781 25001 likely benign 25
924 MYC rs1328542776 SNP missense variant R/H 181 121 0.12 704 possibly damaging 0.703 25001 likely benign 25
925 MYC rs772869147 SNP missense variant G/S 182 381 0.38 19 benign 0.018 21001 likely benign 21
926 MYC rs1449189337 SNP missense variant G/V 182 101 0.1 11 benign 0.01 19001 likely benign 19
927 MYC rs770713291 SNP missense variant S/G 184 611 0.61 11 benign 0.01 11001 likely benign 11
928 MYC rs1414103970 SNP missense variant S/R 184 481 0.48 855 possibly damaging 0.854 18001 likely benign 18
929 MYC rs4645961 SNP missense variant V/I 185 211 0.21 249 benign 0.248 19001 likely benign 19
930 MYC rs1286064895 SNP missense variant C/S 186 791 0.79 8 benign 0.007 23001 likely benign 23
931 MYC rs1469075079 SNP missense variant T/I 188 241 0.24 133 benign 0.132 24001 likely benign 24
932 MYC rs759774541 SNP missense variant S/Y 189 221 0.22 360 benign 0.359 24001 likely benign 24
933 MYC rs1273381542 SNP missense variant L/S 191 761 0.76 79 benign 0.078 23001 likely benign 23
934 MYC rs1273381542 SNP missense variant L/W 191 21 0.02 981 probably damaging 0.98 26001 likely benign 26
935 MYC rs775690959 SNP missense variant Q/P 194 81 0.08 121 benign 0.12 25001 likely benign 25
936 MYC rs775690959 SNP missense variant Q/R 194 201 0.2 884 possibly damaging 0.883 25001 likely benign 25
937 MYC rs1474679499 SNP missense variant A/T 200 41 0.04 330 benign 0.329 25001 likely benign 25
938 MYC rs1425055091 SNP missense variant E/K 202 11 0.01 921 probably damaging 0.92 29001 likely benign 29
939 MYC rs1467496891 SNP missense variant C/Y 203 1 0 1000 probably damaging 0.999 32001 likely deleterious 32
940 MYC rs1174781741 SNP missense variant I/T 204 1 0 969 probably damaging 0.968 32001 likely deleterious 32
941 MYC rs1194568592 SNP missense variant P/L 206 21 0.02 991 probably damaging 0.99 32001 likely deleterious 32
942 MYC rs1221801220 SNP missense variant P/R 213 1 0 1001 probably damaging 1 26001 likely benign 26
943 MYC rs1429861982 SNP missense variant L/F 214 41 0.04 983 probably damaging 0.982 25001 likely benign 25
944 MYC rs753502487 SNP missense variant N/K 215 561 0.56 69 benign 0.068 14001 likely benign 14
945 MYC rs577698378 SNP missense variant D/N 216 71 0.07 653 possibly damaging 0.652 23001 likely benign 23
946 MYC rs778262855 SNP missense variant D/G 216 121 0.12 536 possibly damaging 0.535 22001 likely benign 22
947 MYC rs922203242 SNP missense variant S/N 217 341 0.34 833 possibly damaging 0.832 18001 likely benign 18
948 MYC rs754835412 SNP missense variant S/P 219 291 0.29 215 benign 0.214 22001 likely benign 22
949 MYC rs112602073 SNP missense variant P/S 220 41 0.04 136 benign 0.135 24001 likely benign 24
950 MYC rs1041258616 SNP missense variant P/R 220 41 0.04 902 possibly damaging 0.901 25001 likely benign 25
951 MYC rs758263761 SNP missense variant K/R 221 441 0.44 269 benign 0.268 23001 likely benign 23
952 MYC rs933579368 SNP missense variant K/N 221 331 0.33 19 benign 0.018 22001 likely benign 22
953 MYC rs777695894 SNP missense variant S/T 222 591 0.59 32 benign 0.031 10001 likely benign 10
954 MYC rs1264499327 SNP missense variant A/T 224 251 0.25 4 benign 0.003 6001 likely benign 6
955 MYC rs746958042 SNP missense variant A/V 224 201 0.2 117 benign 0.116 21001 likely benign 21
956 MYC rs770660324 SNP missense variant S/P 225 171 0.17 8 benign 0.007 24001 likely benign 24
957 MYC rs776438693 SNP missense variant S/L 225 141 0.14 8 benign 0.007 23001 likely benign 23
958 MYC rs1174543892 SNP missense variant D/N 227 471 0.47 107 benign 0.106 20001 likely benign 20
959 MYC rs370338821 SNP missense variant S/F 228 61 0.06 448 possibly damaging 0.447 23001 likely benign 23
960 MYC rs1166344892 SNP missense variant S/R 229 511 0.51 58 benign 0.057 11001 likely benign 11
961 MYC rs775427980 SNP missense variant S/T 229 651 0.65 1 benign 0 5001 likely benign 5
962 MYC rs1476455361 SNP missense variant A/T 230 231 0.23 1 benign 0 13001 likely benign 13
963 MYC rs544792311 SNP missense variant A/V 230 201 0.2 1 benign 0 16001 likely benign 16
964 MYC rs1020933770 SNP missense variant S/P 232 221 0.22 14 benign 0.013 24001 likely benign 24
965 MYC rs147506213 SNP missense variant P/T 233 211 0.21 2 benign 0.001 1 likely benign 0
966 MYC rs147506213 SNP missense variant P/A 233 271 0.27 1 benign 0 1 likely benign 0
967 MYC rs147506213 SNP missense variant P/S 233 321 0.32 1 benign 0 1 likely benign 0
968 MYC rs1221550924 SNP missense variant P/Q 233 181 0.18 105 benign 0.104 19001 likely benign 19
969 MYC rs1221550924 SNP missense variant P/L 233 111 0.11 1 benign 0 20001 likely benign 20
970 MYC rs765003654 SNP missense variant L/V 239 541 0.54 377 benign 0.376 23001 likely benign 23
971 MYC rs1000455991 SNP missense variant S/A 240 591 0.59 63 benign 0.062 23001 likely benign 23
972 MYC rs1328290024 SNP missense variant S/P 241 171 0.17 11 benign 0.01 25001 likely benign 25
973 MYC rs186663828 SNP missense variant S/L 241 131 0.13 271 benign 0.27 24001 likely benign 24
974 MYC rs1434118612 SNP missense variant E/K 243 831 0.83 16 benign 0.015 22001 likely benign 22
975 MYC rs1489420810 SNP missense variant E/V 243 271 0.27 16 benign 0.015 22001 likely benign 22
976 MYC rs374701735 SNP missense variant E/D 243 581 0.58 29 benign 0.028 20001 likely benign 20
977 MYC rs545330879 SNP missense variant P/Q 246 101 0.1 657 possibly damaging 0.656 23001 likely benign 23
978 MYC rs545330879 SNP missense variant P/R 246 141 0.14 584 possibly damaging 0.583 23001 likely benign 23
979 MYC rs545330879 SNP missense variant P/L 246 41 0.04 274 benign 0.273 24001 likely benign 24
980 MYC rs1362563336 SNP missense variant G/D 248 551 0.55 60 benign 0.059 17001 likely benign 17
981 MYC rs1362563336 SNP missense variant G/V 248 431 0.43 16 benign 0.015 18001 likely benign 18
982 MYC rs772761233 SNP missense variant S/N 249 191 0.19 7 benign 0.006 21001 likely benign 21
983 MYC rs1367173254 SNP missense variant P/L 250 171 0.17 148 benign 0.147 23001 likely benign 23
984 MYC rs766666917 SNP missense variant E/K 251 671 0.67 4 benign 0.003 17001 likely benign 17
985 MYC rs752344761 SNP missense variant P/H 252 91 0.09 4 benign 0.003 22001 likely benign 22
986 MYC rs763627051 SNP missense variant L/P 253 291 0.29 534 possibly damaging 0.533 16001 likely benign 16
987 MYC rs751130055 SNP missense variant V/M 254 171 0.17 2 benign 0.001 21001 likely benign 21
988 MYC rs757183481 SNP missense variant L/F 255 711 0.71 963 probably damaging 0.962 18001 likely benign 18
989 MYC rs781041285 SNP missense variant H/D 256 651 0.65 30 benign 0.029 17001 likely benign 17
990 MYC rs750374321 SNP missense variant H/P 256 291 0.29 1 benign 0 17001 likely benign 17
991 MYC rs750374321 SNP missense variant H/R 256 501 0.5 30 benign 0.029 15001 likely benign 15
992 MYC rs779748283 SNP missense variant H/Q 256 561 0.56 4 benign 0.003 3001 likely benign 3
993 MYC rs1467095827 SNP missense variant E/K 258 121 0.12 110 benign 0.109 23001 likely benign 23
994 MYC rs1057519851 SNP missense variant P/A 260 561 0.56 326 benign 0.325 22001 likely benign 22
995 MYC rs749498067 SNP missense variant P/Q 260 411 0.41 102 benign 0.101 23001 likely benign 23
996 MYC rs1020542388 SNP missense variant T/I 263 31 0.03 226 benign 0.225 26001 likely benign 26
997 MYC rs1159672918 SNP missense variant S/C 264 91 0.09 907 possibly damaging 0.906 25001 likely benign 25
998 MYC rs1442840229 SNP missense variant S/I 264 91 0.09 879 possibly damaging 0.878 26001 likely benign 26
999 MYC rs1209695374 SNP missense variant E/D 269 191 0.19 35 benign 0.034 21001 likely benign 21
1000 MYC rs977518778 SNP missense variant E/K 274 11 0.01 170 benign 0.169 28001 likely benign 28
1001 MYC rs1358102215 SNP missense variant D/N 278 1 0 999 probably damaging 0.998 32001 likely deleterious 32
1002 MYC rs1195526437 SNP missense variant V/L 280 1 0 995 probably damaging 0.994 28001 likely benign 28
1003 MYC rs1426971261 SNP missense variant V/M 282 1 0 908 possibly damaging 0.907 31001 likely deleterious 31
1004 MYC rs1355624510 SNP missense variant V/A 282 11 0.01 649 possibly damaging 0.648 29001 likely benign 29
1005 MYC rs1413496327 SNP missense variant E/G 283 1 0 105 benign 0.104 32001 likely deleterious 32
1006 MYC rs755221038 SNP missense variant K/M 284 1 0 232 benign 0.231 29001 likely benign 29
1007 MYC rs756770497 SNP missense variant K/N 284 1 0 776 possibly damaging 0.775 28001 likely benign 28
1008 MYC rs1563758692 SNP missense variant R/K 285 21 0.02 343 benign 0.342 28001 likely benign 28
1009 MYC rs1437137562 SNP missense variant Q/E 286 191 0.19 138 benign 0.137 23001 likely benign 23
1010 MYC rs772229477 SNP missense variant Q/L 286 21 0.02 8 benign 0.007 28001 likely benign 28
1011 MYC rs778030574 SNP missense variant G/C 289 31 0.03 7 benign 0.006 23001 likely benign 23
1012 MYC rs747518067 SNP missense variant E/V 293 331 0.33 20 benign 0.019 24001 likely benign 24
1013 MYC rs562953156 SNP missense variant S/L 296 71 0.07 345 benign 0.344 22001 likely benign 22
1014 MYC rs150629172 SNP missense variant P/H 297 181 0.18 1 benign 0 14001 likely benign 14
1015 MYC rs770159089 SNP missense variant A/S 299 941 0.94 2 benign 0.001 1 likely benign 0
1016 MYC rs372210680 SNP missense variant G/D 301 291 0.29 4 benign 0.003 19001 likely benign 19
1017 MYC rs1285441185 SNP missense variant H/R 302 361 0.36 230 benign 0.229 16001 likely benign 16
1018 MYC rs139697494 SNP missense variant H/Q 302 291 0.29 42 benign 0.041 16001 likely benign 16
1019 MYC rs766987302 SNP missense variant S/R 303 311 0.31 161 benign 0.16 20001 likely benign 20
1020 MYC rs772650309 SNP missense variant K/I 304 11 0.01 406 benign 0.405 23001 likely benign 23
1021 MYC rs760650253 SNP missense variant P/H 305 141 0.14 972 probably damaging 0.971 22001 likely benign 22
1022 MYC rs760650253 SNP missense variant P/R 305 91 0.09 963 probably damaging 0.962 22001 likely benign 22
1023 MYC rs766292378 SNP missense variant P/L 306 161 0.16 6 benign 0.005 22001 likely benign 22
1024 MYC rs781657156 SNP missense variant L/P 312 1 0 985 probably damaging 0.984 32001 likely deleterious 32
1025 MYC rs1157474201 SNP missense variant K/R 313 11 0.01 995 probably damaging 0.994 31001 likely deleterious 31
1026 MYC rs1380388393 SNP missense variant R/W 314 21 0.02 1000 probably damaging 0.999 23001 likely benign 23
1027 MYC rs1179847000 SNP missense variant C/F 315 1 0 936 probably damaging 0.935 31001 likely deleterious 31
1028 MYC rs1051420663 SNP missense variant H/R 316 41 0.04 998 probably damaging 0.997 28001 likely benign 28
1029 MYC rs752926420 SNP missense variant V/F 317 21 0.02 980 probably damaging 0.979 29001 likely benign 29
1030 MYC rs1490057941 SNP missense variant S/C 318 51 0.05 795 possibly damaging 0.794 24001 likely benign 24
1031 MYC rs903134011 SNP missense variant H/L 320 11 0.01 919 probably damaging 0.918 28001 likely benign 28
1032 MYC rs146971340 SNP missense variant H/Q 320 561 0.56 328 benign 0.327 10001 likely benign 10
1033 MYC rs781494801 SNP missense variant P/S 327 121 0.12 69 benign 0.068 20001 likely benign 20
1034 MYC rs1354508987 SNP missense variant P/A 328 51 0.05 998 probably damaging 0.997 23001 likely benign 23
1035 MYC rs1272045308 SNP missense variant S/P 329 231 0.23 975 probably damaging 0.974 23001 likely benign 23
1036 MYC rs746409847 SNP missense variant T/P 330 81 0.08 906 possibly damaging 0.905 25001 likely benign 25
1037 MYC rs746409847 SNP missense variant T/A 330 111 0.11 407 benign 0.406 24001 likely benign 24
1038 MYC rs184271012 SNP missense variant R/W 331 1 0 901 possibly damaging 0.9 23001 likely benign 23
1039 MYC rs772772048 SNP missense variant R/Q 331 41 0.04 238 benign 0.237 31001 likely deleterious 31
1040 MYC rs1479419101 SNP missense variant P/T 335 1 0 914 probably damaging 0.913 24001 likely benign 24
1041 MYC rs1177628089 SNP missense variant P/L 335 1 0 767 possibly damaging 0.766 23001 likely benign 23
1042 MYC rs1378948166 SNP missense variant A/S 337 171 0.17 29 benign 0.028 16001 likely benign 16
1043 MYC rs4645968 SNP missense variant A/V 337 1001 1 10 benign 0.009 20001 likely benign 20
1044 MYC rs893110546 SNP missense variant K/R 341 281 0.28 7 benign 0.006 22001 likely benign 22
1045 MYC rs765924453 SNP missense variant D/N 343 91 0.09 965 probably damaging 0.964 24001 likely benign 24
1046 MYC rs776379651 SNP missense variant D/E 343 1001 1 184 benign 0.183 19001 likely benign 19
1047 MYC rs1236689606 SNP missense variant S/G 344 181 0.18 4 benign 0.003 24001 likely benign 24
1048 MYC rs773571686 SNP missense variant S/N 344 161 0.16 16 benign 0.015 22001 likely benign 22
1049 MYC rs773571686 SNP missense variant S/I 344 41 0.04 736 possibly damaging 0.735 26001 likely benign 26
1050 MYC rs752586995 SNP missense variant R/T 346 61 0.06 390 benign 0.389 23001 likely benign 23
1051 MYC rs758679560 SNP missense variant R/T 349 11 0.01 1 benign 0 23001 likely benign 23
1052 MYC rs764346243 SNP missense variant I/M 351 11 0.01 998 probably damaging 0.997 26001 likely benign 26
1053 MYC rs1013179067 SNP missense variant S/T 352 281 0.28 916 probably damaging 0.915 23001 likely benign 23
1054 MYC rs1313047247 SNP missense variant N/K 354 411 0.41 998 probably damaging 0.997 23001 likely benign 23
1055 MYC rs1415460536 SNP missense variant K/E 356 1 0 170 benign 0.169 25001 likely benign 25
1056 MYC rs1355490965 SNP missense variant C/S 357 501 0.5 997 probably damaging 0.996 24001 likely benign 24
1057 MYC rs1355490965 SNP missense variant C/G 357 31 0.03 997 probably damaging 0.996 29001 likely benign 29
1058 MYC rs1012972478 SNP missense variant C/Y 357 1 0 999 probably damaging 0.998 32001 likely deleterious 32
1059 MYC rs1012972478 SNP missense variant C/F 357 1 0 998 probably damaging 0.997 32001 likely deleterious 32
1060 MYC rs1480367143 SNP missense variant S/N 359 1 0 998 probably damaging 0.997 30001 likely deleterious 30
1061 MYC rs751822114 SNP missense variant R/G 361 31 0.03 997 probably damaging 0.996 23001 likely benign 23
1062 MYC rs1024952766 SNP missense variant R/S 361 1 0 997 probably damaging 0.996 26001 likely benign 26
1063 MYC rs200431478 SNP missense variant S/C 362 11 0.01 936 probably damaging 0.935 27001 likely benign 27
1064 MYC rs200431478 SNP missense variant S/F 362 1 0 915 probably damaging 0.914 27001 likely benign 27
1065 MYC rs1197838517 SNP missense variant D/N 364 1 0 999 probably damaging 0.998 25001 likely benign 25
1066 MYC rs746333391 SNP missense variant D/V 364 1 0 1000 probably damaging 0.999 27001 likely benign 27
1067 MYC rs756666851 SNP missense variant E/K 366 1 0 998 probably damaging 0.997 32001 likely deleterious 32
1068 MYC rs749722454 SNP missense variant E/K 367 11 0.01 737 possibly damaging 0.736 32001 likely deleterious 32
1069 MYC rs769010031 SNP missense variant N/T 368 21 0.02 311 benign 0.31 26001 likely benign 26
1070 MYC rs878873271 SNP missense variant R/Q 372 11 0.01 964 probably damaging 0.963 32001 likely deleterious 32
1071 MYC rs878873271 SNP missense variant R/L 372 21 0.02 769 possibly damaging 0.768 32001 likely deleterious 32
1072 MYC rs777230092 SNP missense variant N/K 375 1 0 1000 probably damaging 0.999 24001 likely benign 24
1073 MYC rs1276187525 SNP missense variant V/I 376 471 0.47 306 benign 0.305 24001 likely benign 24
1074 MYC rs1401250556 SNP missense variant Q/H 380 1 0 999 probably damaging 0.998 27001 likely benign 27
1075 MYC rs776244909 SNP missense variant R/Q 387 31 0.03 370 benign 0.369 32001 likely deleterious 32
1076 MYC rs1460956206 SNP missense variant F/C 390 1 0 981 probably damaging 0.98 32001 likely deleterious 32
1077 MYC rs771168413 SNP missense variant D/H 394 1 0 1000 probably damaging 0.999 32001 likely deleterious 32
1078 MYC rs771168413 SNP missense variant D/Y 394 21 0.02 1000 probably damaging 0.999 32001 likely deleterious 32
1079 MYC rs141095253 SNP missense variant P/L 397 31 0.03 1000 probably damaging 0.999 28001 likely benign 28
1080 MYC rs762139580 SNP missense variant A/S 405 11 0.01 998 probably damaging 0.997 29001 likely benign 29
1081 MYC rs1442494202 SNP missense variant P/S 406 131 0.13 174 benign 0.173 22001 likely benign 22
1082 MYC rs767477446 SNP missense variant K/I 412 1 0 985 probably damaging 0.984 29001 likely benign 29
1083 MYC rs750562100 SNP missense variant T/I 415 41 0.04 863 possibly damaging 0.862 25001 likely benign 25
1084 MYC rs756611896 SNP missense variant A/T 416 11 0.01 1 benign 0 18001 likely benign 18
1085 MYC rs1193335325 SNP missense variant A/V 416 11 0.01 1 benign 0 22001 likely benign 22
1086 MYC rs755283006 SNP missense variant V/I 421 871 0.87 1 benign 0 1 likely benign 0
1087 MYC rs1332562282 SNP missense variant A/T 423 251 0.25 4 benign 0.003 16001 likely benign 16
1088 MYC rs1415084652 SNP missense variant E/A 424 11 0.01 54 benign 0.053 23001 likely benign 23
1089 MYC rs1336293145 SNP missense variant E/G 425 1 0 711 possibly damaging 0.71 32001 likely deleterious 32
1090 MYC rs746611175 SNP missense variant L/F 428 1 0 1000 probably damaging 0.999 26001 likely benign 26
1091 MYC rs1389942859 SNP missense variant E/K 432 1001 1 1 benign 0 19001 likely benign 19
1092 MYC rs553965730 SNP missense variant D/G 433 11 0.01 20 benign 0.019 25001 likely benign 25
1093 MYC rs145561065 SNP missense variant L/F 434 31 0.03 101 benign 0.1 19001 likely benign 19
1094 MYC rs145561065 SNP missense variant L/F 434 31 0.03 101 benign 0.1 19001 likely benign 19
1095 MYC rs774254150 SNP missense variant R/W 436 1 0 630 possibly damaging 0.629 23001 likely benign 23
1096 MYC rs761932135 SNP missense variant R/Q 436 461 0.46 6 benign 0.005 24001 likely benign 24
1097 MYC rs1465173750 SNP missense variant R/Q 438 11 0.01 105 benign 0.104 24001 likely benign 24
1098 MYC rs148863193 SNP missense variant R/Q 439 591 0.59 8 benign 0.007 22001 likely benign 22
1099 MYC rs148863193 SNP missense variant R/L 439 121 0.12 194 benign 0.193 23001 likely benign 23
1100 MYC rs750651389 SNP missense variant E/V 440 1 0 383 benign 0.382 27001 likely benign 27
1101 MYC rs760686595 SNP missense variant L/F 442 1 0 1000 probably damaging 0.999 23001 likely benign 23
1102 MYC rs370767192 SNP missense variant H/Y 444 31 0.03 37 benign 0.036 23001 likely benign 23
1103 MYC rs754298537 SNP missense variant K/E 445 1 0 292 benign 0.291 25001 likely benign 25
1104 MYC rs755545316 SNP missense variant E/G 447 11 0.01 155 benign 0.154 24001 likely benign 24
1105 MYC rs1478499127 SNP missense variant Q/R 448 181 0.18 7 benign 0.006 23001 likely benign 23
1106 MYC rs779123478 SNP missense variant R/G 450 1 0 458 possibly damaging 0.457 26001 likely benign 26
1107 MYC rs779123478 SNP missense variant R/W 450 1 0 863 possibly damaging 0.862 29001 likely benign 29
1108 MYC rs201337668 SNP missense variant C/G 453 631 0.63 1 benign 0 18001 likely benign 18
1109 MYC rs536396530 SNP missense variant C/S 453 701 0.7 10 benign 0.009 19001 likely benign 19
1110 MYC rs536396530 SNP missense variant C/F 453 141 0.14 82 benign 0.081 22001 likely benign 22
1111 MYC rs143501729 SNP missense variant A/E 454 1 0 15 benign 0.014 22001 likely benign 22
1112 CCND1 rs572037183 SNP missense variant E/K 2 141 0.14 13 benign 0.012 23001 likely benign 23
1113 CCND1 rs572037183 SNP missense variant E/Q 2 171 0.17 52 benign 0.051 23001 likely benign 23
1114 CCND1 rs545664320 SNP missense variant H/R 3 151 0.15 24 benign 0.023 21001 likely benign 21
1115 CCND1 rs1356268873 SNP missense variant Q/H 4 1 0 309 benign 0.308 24001 likely benign 24
1116 CCND1 rs993495966 SNP missense variant C/S 7 1 0 980 probably damaging 0.979 28001 likely benign 28
1117 CCND1 rs993495966 SNP missense variant C/R 7 1 0 995 probably damaging 0.994 31001 likely deleterious 31
1118 CCND1 rs1486252402 SNP missense variant C/S 7 1 0 980 probably damaging 0.979 28001 likely benign 28
1119 CCND1 rs773884084 SNP missense variant C/G 8 41 0.04 72 benign 0.071 24001 likely benign 24
1120 CCND1 rs1340132260 SNP missense variant C/Y 8 81 0.08 710 possibly damaging 0.709 25001 likely benign 25
1121 CCND1 rs761266790 SNP missense variant V/M 10 171 0.17 2 benign 0.001 23001 likely benign 23
1122 CCND1 rs1372181670 SNP missense variant R/S 14 591 0.59 174 benign 0.173 22001 likely benign 22
1123 CCND1 rs557545630 SNP missense variant R/S 15 1 0 899 possibly damaging 0.898 27001 likely benign 27
1124 CCND1 rs1299107729 SNP missense variant A/S 16 51 0.05 902 possibly damaging 0.901 25001 likely benign 25
1125 CCND1 rs772857967 SNP missense variant P/A 18 641 0.64 1 benign 0 20001 likely benign 20
1126 CCND1 rs772857967 SNP missense variant P/S 18 661 0.66 1 benign 0 21001 likely benign 21
1127 CCND1 rs1417631865 SNP missense variant D/E 19 31 0.03 949 probably damaging 0.948 25001 likely benign 25
1128 CCND1 rs766170770 SNP missense variant N/D 21 371 0.37 266 benign 0.265 23001 likely benign 23
1129 CCND1 rs753863475 SNP missense variant L/F 23 31 0.03 19 benign 0.018 23001 likely benign 23
1130 CCND1 rs1400812649 SNP missense variant D/G 25 1 0 761 possibly damaging 0.76 32001 likely deleterious 32
1131 CCND1 rs2220247 SNP missense variant A/T 30 411 0.41 4 benign 0.003 22001 likely benign 22
1132 CCND1 rs2220247 SNP missense variant A/S 30 421 0.42 12 benign 0.011 22001 likely benign 22
1133 CCND1 rs1415272481 SNP missense variant A/D 30 41 0.04 590 possibly damaging 0.589 26001 likely benign 26
1134 CCND1 rs746088878 SNP missense variant E/K 36 41 0.04 133 benign 0.132 26001 likely benign 26
1135 CCND1 rs1482952019 SNP missense variant E/D 36 401 0.4 8 benign 0.007 22001 likely benign 22
1136 CCND1 rs1263446681 SNP missense variant T/S 37 31 0.03 11 benign 0.01 23001 likely benign 23
1137 CCND1 rs780366497 SNP missense variant C/W 38 21 0.02 952 probably damaging 0.951 27001 likely benign 27
1138 CCND1 rs749614691 SNP missense variant S/L 41 131 0.13 302 benign 0.301 23001 likely benign 23
1139 CCND1 rs1173840555 SNP missense variant F/L 45 21 0.02 88 benign 0.087 24001 likely benign 24
1140 CCND1 rs747665638 SNP missense variant K/E 46 131 0.13 76 benign 0.075 23001 likely benign 23
1141 CCND1 rs1332727287 SNP missense variant K/E 50 71 0.07 26 benign 0.025 24001 likely benign 24
1142 CCND1 rs1565224527 SNP missense variant K/N 50 51 0.05 47 benign 0.046 24001 likely benign 24
1143 CCND1 rs772785280 SNP missense variant E/D 51 1001 1 4 benign 0.003 18001 likely benign 18
1144 CCND1 rs760341225 SNP missense variant P/R 54 1 0 995 probably damaging 0.994 28001 likely benign 28
1145 CCND1 rs765904377 SNP missense variant M/L 56 21 0.02 97 benign 0.096 24001 likely benign 24
1146 CCND1 rs748632355 SNP missense variant T/N 62 231 0.23 43 benign 0.042 22001 likely benign 22
1147 CCND1 rs748632355 SNP missense variant T/I 62 301 0.3 495 possibly damaging 0.494 24001 likely benign 24
1148 CCND1 rs1299820976 SNP missense variant M/L 64 41 0.04 198 benign 0.197 25001 likely benign 25
1149 CCND1 rs759345822 SNP missense variant E/A 66 1 0 933 probably damaging 0.932 34001 likely deleterious 34
1150 CCND1 rs759345822 SNP missense variant E/G 66 1 0 976 probably damaging 0.975 35001 likely deleterious 35
1151 CCND1 rs1565224976 SNP missense variant V/I 67 21 0.02 689 possibly damaging 0.688 33001 likely deleterious 33
1152 CCND1 rs769045064 SNP missense variant E/G 69 1 0 98 benign 0.097 29001 likely benign 29
1153 CCND1 rs1381472659 SNP missense variant E/K 74 11 0.01 148 benign 0.147 27001 likely benign 27
1154 CCND1 rs1171564865 SNP missense variant E/K 75 11 0.01 136 benign 0.135 27001 likely benign 27
1155 CCND1 rs778080996 SNP missense variant E/K 76 11 0.01 256 benign 0.255 27001 likely benign 27
1156 CCND1 rs746530862 SNP missense variant E/D 76 231 0.23 7 benign 0.006 19001 likely benign 19
1157 CCND1 rs781047821 SNP missense variant P/S 79 11 0.01 711 possibly damaging 0.71 27001 likely benign 27
1158 CCND1 rs1188165799 SNP missense variant A/T 81 1 0 416 benign 0.415 26001 likely benign 26
1159 CCND1 rs1471534715 SNP missense variant M/V 82 251 0.25 15 benign 0.014 20001 likely benign 20
1160 CCND1 rs1359042394 SNP missense variant P/T 93 61 0.06 35 benign 0.034 22001 likely benign 22
1161 CCND1 rs1359042394 SNP missense variant P/S 93 91 0.09 26 benign 0.025 22001 likely benign 22
1162 CCND1 rs1419585038 SNP missense variant P/L 93 11 0.01 212 benign 0.211 25001 likely benign 25
1163 CCND1 rs774091629 SNP missense variant V/L 94 431 0.43 8 benign 0.007 19001 likely benign 19
1164 CCND1 rs760878237 SNP missense variant K/N 95 81 0.08 59 benign 0.058 20001 likely benign 20
1165 CCND1 rs148113872 SNP missense variant K/N 96 1 0 992 probably damaging 0.991 31001 likely deleterious 31
1166 CCND1 rs148113872 SNP missense variant K/N 96 1 0 992 probably damaging 0.991 31001 likely deleterious 31
1167 CCND1 rs140967247 SNP missense variant R/S 98 341 0.34 102 benign 0.101 23001 likely benign 23
1168 CCND1 rs1480433568 SNP missense variant L/R 101 1 0 960 probably damaging 0.959 32001 likely deleterious 32
1169 CCND1 rs753115532 SNP missense variant A/T 104 111 0.11 409 benign 0.408 24001 likely benign 24
1170 CCND1 rs753115532 SNP missense variant A/S 104 231 0.23 481 possibly damaging 0.48 25001 likely benign 25
1171 CCND1 rs764727750 SNP missense variant M/L 107 321 0.32 20 benign 0.019 23001 likely benign 23
1172 CCND1 rs751995000 SNP missense variant F/L 108 341 0.34 50 benign 0.049 22001 likely benign 22
1173 CCND1 rs374998781 SNP missense variant K/R 114 521 0.52 36 benign 0.035 22001 likely benign 22
1174 CCND1 rs755854763 SNP missense variant I/N 117 441 0.44 58 benign 0.057 23001 likely benign 23
1175 CCND1 rs1176401077 SNP missense variant I/M 117 271 0.27 101 benign 0.1 18001 likely benign 18
1176 CCND1 rs1469991905 SNP missense variant A/T 121 51 0.05 496 possibly damaging 0.495 25001 likely benign 25
1177 CCND1 rs768334579 SNP missense variant E/K 122 21 0.02 382 benign 0.381 26001 likely benign 26
1178 CCND1 rs1373598994 SNP missense variant E/G 122 1 0 313 benign 0.312 26001 likely benign 26
1179 CCND1 rs1449765247 SNP missense variant K/Q 123 61 0.06 490 possibly damaging 0.489 25001 likely benign 25
1180 CCND1 rs774409065 SNP missense variant K/M 123 1 0 655 possibly damaging 0.654 31001 likely deleterious 31
1181 CCND1 rs748059951 SNP missense variant L/P 124 1 0 1001 probably damaging 1 32001 likely deleterious 32
1182 CCND1 rs1565225031 SNP missense variant C/R 125 1 0 996 probably damaging 0.995 31001 likely deleterious 31
1183 CCND1 rs1329584649 SNP missense variant I/L 126 41 0.04 26 benign 0.025 24001 likely benign 24
1184 CCND1 rs1375845153 SNP missense variant Y/H 127 1 0 974 probably damaging 0.973 32001 likely deleterious 32
1185 CCND1 rs1312761797 SNP missense variant T/A 128 21 0.02 374 benign 0.373 25001 likely benign 25
1186 CCND1 rs771952150 SNP missense variant D/N 129 11 0.01 509 possibly damaging 0.508 32001 likely deleterious 32
1187 CCND1 rs1050971 SNP missense variant N/D 130 11 0.01 215 benign 0.214 24001 likely benign 24
1188 CCND1 rs1050971 SNP missense variant N/Y 130 81 0.08 84 benign 0.083 23001 likely benign 23
1189 CCND1 rs1131439 SNP missense variant N/S 130 81 0.08 56 benign 0.055 23001 likely benign 23
1190 CCND1 rs759551813 SNP missense variant S/F 131 1 0 836 possibly damaging 0.835 29001 likely benign 29
1191 CCND1 rs866931401 SNP missense variant R/Q 133 401 0.4 1 benign 0 19001 likely benign 19
1192 CCND1 rs866931401 SNP missense variant R/L 133 211 0.21 1 benign 0 20001 likely benign 20
1193 CCND1 rs765498502 SNP missense variant P/S 134 161 0.16 55 benign 0.054 23001 likely benign 23
1194 CCND1 rs763443319 SNP missense variant E/K 135 461 0.46 4 benign 0.003 23001 likely benign 23
1195 CCND1 rs764335132 SNP missense variant E/V 135 101 0.1 15 benign 0.014 23001 likely benign 23
1196 CCND1 rs1184664065 SNP missense variant E/A 136 11 0.01 433 benign 0.432 27001 likely benign 27
1197 CCND1 rs900779300 SNP missense variant E/D 136 161 0.16 16 benign 0.015 22001 likely benign 22
1198 CCND1 rs752157015 SNP missense variant L/M 137 41 0.04 904 possibly damaging 0.903 24001 likely benign 24
1199 CCND1 rs1268871232 SNP missense variant Q/H 139 31 0.03 4 benign 0.003 23001 likely benign 23
1200 CCND1 rs1260695584 SNP missense variant L/F 143 71 0.07 332 benign 0.331 21001 likely benign 21
1201 CCND1 rs766855822 SNP missense variant L/P 143 11 0.01 396 benign 0.395 28001 likely benign 28
1202 CCND1 rs753296773 SNP missense variant L/V 144 1001 1 1 benign 0 16001 likely benign 16
1203 CCND1 rs374420164 SNP missense variant L/F 148 1 0 1000 probably damaging 0.999 27001 likely benign 27
1204 CCND1 rs1203615889 SNP missense variant L/M 152 91 0.09 921 probably damaging 0.92 22001 likely benign 22
1205 CCND1 rs752345237 SNP missense variant A/P 154 1 0 824 possibly damaging 0.823 24001 likely benign 24
1206 CCND1 rs752345237 SNP missense variant A/S 154 421 0.42 95 benign 0.094 17001 likely benign 17
1207 CCND1 rs1292226646 SNP missense variant M/V 155 1001 1 1 benign 0 11001 likely benign 11
1208 CCND1 rs1565225289 SNP missense variant T/I 156 411 0.41 991 probably damaging 0.99 23001 likely benign 23
1209 CCND1 rs1565225292 SNP missense variant H/Y 158 191 0.19 13 benign 0.012 22001 likely benign 22
1210 CCND1 rs11263523 SNP missense variant H/Q 158 111 0.11 44 benign 0.043 18001 likely benign 18
1211 CCND1 rs11263523 SNP missense variant H/Q 158 111 0.11 44 benign 0.043 18001 likely benign 18
1212 CCND1 rs781118003 SNP missense variant D/N 159 1 0 874 possibly damaging 0.873 32001 likely deleterious 32
1213 CCND1 rs749340325 SNP missense variant D/G 159 21 0.02 913 probably damaging 0.912 32001 likely deleterious 32
1214 CCND1 rs1447014281 SNP missense variant I/M 161 11 0.01 652 possibly damaging 0.651 23001 likely benign 23
1215 CCND1 rs1332977808 SNP missense variant E/G 162 31 0.03 108 benign 0.107 26001 likely benign 26
1216 CCND1 rs768767169 SNP missense variant H/R 163 11 0.01 512 possibly damaging 0.511 26001 likely benign 26
1217 CCND1 rs537363548 SNP missense variant F/L 164 101 0.1 62 benign 0.061 23001 likely benign 23
1218 CCND1 rs1432185835 SNP missense variant L/V 165 71 0.07 462 possibly damaging 0.461 24001 likely benign 24
1219 CCND1 rs1261290754 SNP missense variant P/S 169 141 0.14 92 benign 0.091 23001 likely benign 23
1220 CCND1 rs548963461 SNP missense variant E/V 170 341 0.34 1 benign 0 23001 likely benign 23
1221 CCND1 rs747336419 SNP missense variant E/D 170 81 0.08 1 benign 0 22001 likely benign 22
1222 CCND1 rs1565225324 SNP missense variant A/P 171 1001 1 1 benign 0 19001 likely benign 19
1223 CCND1 rs1373641771 SNP missense variant A/V 171 161 0.16 2 benign 0.001 22001 likely benign 22
1224 CCND1 rs374062310 SNP missense variant N/K 174 1001 1 16 benign 0.015 19001 likely benign 19
1225 CCND1 rs1175448240 SNP missense variant K/E 175 981 0.98 26 benign 0.025 22001 likely benign 22
1226 CCND1 rs777185874 SNP missense variant Q/E 176 1001 1 4 benign 0.003 19001 likely benign 19
1227 CCND1 rs1433903280 SNP missense variant Q/L 176 311 0.31 2 benign 0.001 23001 likely benign 23
1228 CCND1 rs143479406 SNP missense variant R/H 179 11 0.01 836 possibly damaging 0.835 33001 likely deleterious 33
1229 CCND1 rs143479406 SNP missense variant R/L 179 41 0.04 937 probably damaging 0.936 32001 likely deleterious 32
1230 CCND1 rs1176469241 SNP missense variant H/Q 181 1 0 871 possibly damaging 0.87 23001 likely benign 23
1231 CCND1 rs1434771092 SNP missense variant Q/K 183 21 0.02 663 possibly damaging 0.662 26001 likely benign 26
1232 CCND1 rs1173908293 SNP missense variant T/S 184 71 0.07 290 benign 0.289 22001 likely benign 22
1233 CCND1 rs763697017 SNP missense variant V/I 186 1001 1 24 benign 0.023 22001 likely benign 22
1234 CCND1 rs1252289930 SNP missense variant A/V 187 11 0.01 598 possibly damaging 0.597 28001 likely benign 28
1235 CCND1 rs751315372 SNP missense variant L/F 188 1 0 622 possibly damaging 0.621 26001 likely benign 26
1236 CCND1 rs757229078 SNP missense variant C/Y 189 1 0 998 probably damaging 0.997 32001 likely deleterious 32
1237 CCND1 rs534553548 SNP missense variant A/S 190 41 0.04 602 possibly damaging 0.601 29001 likely benign 29
1238 CCND1 rs201012923 SNP missense variant V/M 193 181 0.18 45 benign 0.044 22001 likely benign 22
1239 CCND1 rs1282637304 SNP missense variant K/N 194 331 0.33 152 benign 0.151 21001 likely benign 21
1240 CCND1 rs759570740 SNP missense variant N/S 198 351 0.35 4 benign 0.003 20001 likely benign 20
1241 CCND1 rs1222442441 SNP missense variant P/L 199 31 0.03 831 possibly damaging 0.83 26001 likely benign 26
1242 CCND1 rs1353308163 SNP missense variant P/S 200 1 0 992 probably damaging 0.991 25001 likely benign 25
1243 CCND1 rs893823618 SNP missense variant V/L 203 41 0.04 13 benign 0.012 23001 likely benign 23
1244 CCND1 rs751664590 SNP missense variant A/T 204 1 0 985 probably damaging 0.984 26001 likely benign 26
1245 CCND1 rs1193747086 SNP missense variant A/S 205 151 0.15 785 possibly damaging 0.784 23001 likely benign 23
1246 CCND1 rs1271260640 SNP missense variant A/V 205 11 0.01 859 possibly damaging 0.858 25001 likely benign 25
1247 CCND1 rs1011426441 SNP missense variant V/M 208 121 0.12 478 possibly damaging 0.477 23001 likely benign 23
1248 CCND1 rs750639632 SNP missense variant V/A 209 1001 1 2 benign 0.001 18001 likely benign 18
1249 CCND1 rs756509430 SNP missense variant A/T 211 1 0 996 probably damaging 0.995 29001 likely benign 29
1250 CCND1 rs112525097 SNP missense variant N/K 216 671 0.67 10 benign 0.009 17001 likely benign 17
1251 CCND1 rs149457002 SNP missense variant S/N 219 371 0.37 2 benign 0.001 18001 likely benign 18
1252 CCND1 rs1404273153 SNP missense variant P/S 220 971 0.97 1 benign 0 2001 likely benign 2
1253 CCND1 rs747703578 SNP missense variant P/L 220 391 0.39 1 benign 0 20001 likely benign 20
1254 CCND1 rs1412188214 SNP missense variant N/H 221 81 0.08 237 benign 0.236 20001 likely benign 20
1255 CCND1 rs746640562 SNP missense variant L/M 224 161 0.16 44 benign 0.043 22001 likely benign 22
1256 CCND1 rs776600964 SNP missense variant Y/C 226 181 0.18 1 benign 0 21001 likely benign 21
1257 CCND1 rs776600964 SNP missense variant Y/F 226 691 0.69 8 benign 0.007 16001 likely benign 16
1258 CCND1 rs1222446202 SNP missense variant R/C 228 71 0.07 13 benign 0.012 22001 likely benign 22
1259 CCND1 rs200179137 SNP missense variant R/H 228 141 0.14 2 benign 0.001 23001 likely benign 23
1260 CCND1 rs984643266 SNP missense variant T/K 230 11 0.01 914 probably damaging 0.913 26001 likely benign 26
1261 CCND1 rs984643266 SNP missense variant T/I 230 271 0.27 292 benign 0.291 22001 likely benign 22
1262 CCND1 rs745779714 SNP missense variant R/S 231 231 0.23 8 benign 0.007 16001 likely benign 16
1263 CCND1 rs745779714 SNP missense variant R/G 231 161 0.16 4 benign 0.003 17001 likely benign 17
1264 CCND1 rs745779714 SNP missense variant R/C 231 71 0.07 578 possibly damaging 0.577 23001 likely benign 23
1265 CCND1 rs1228811654 SNP missense variant L/I 233 31 0.03 961 probably damaging 0.96 26001 likely benign 26
1266 CCND1 rs1165177408 SNP missense variant S/T 234 201 0.2 12 benign 0.011 22001 likely benign 22
1267 CCND1 rs773470948 SNP missense variant I/M 237 41 0.04 946 probably damaging 0.945 23001 likely benign 23
1268 CCND1 rs1423874357 SNP missense variant K/Q 238 441 0.44 2 benign 0.001 22001 likely benign 22
1269 CCND1 rs760907398 SNP missense variant K/N 238 831 0.83 2 benign 0.001 20001 likely benign 20
1270 CCND1 rs777225097 SNP missense variant P/L 241 381 0.38 4 benign 0.003 24001 likely benign 24
1271 CCND1 rs913470506 SNP missense variant R/W 245 1 0 974 probably damaging 0.973 31001 likely deleterious 31
1272 CCND1 rs1565073727 SNP missense variant R/Q 245 91 0.09 73 benign 0.072 24001 likely benign 24
1273 CCND1 rs925960764 SNP missense variant A/S 246 171 0.17 53 benign 0.052 22001 likely benign 22
1274 CCND1 rs1417190579 SNP missense variant C/Y 247 1 0 997 probably damaging 0.996 32001 likely deleterious 32
1275 CCND1 rs1417190579 SNP missense variant C/F 247 1 0 1000 probably damaging 0.999 32001 likely deleterious 32
1276 CCND1 rs1446903472 SNP missense variant Q/K 250 21 0.02 676 possibly damaging 0.675 25001 likely benign 25
1277 CCND1 rs1377678585 SNP missense variant Q/R 250 31 0.03 637 possibly damaging 0.636 26001 likely benign 26
1278 CCND1 rs1173812710 SNP missense variant E/K 252 1 0 992 probably damaging 0.991 32001 likely deleterious 32
1279 CCND1 rs750012493 SNP missense variant S/T 258 1 0 169 benign 0.168 24001 likely benign 24
1280 CCND1 rs755986542 SNP missense variant R/C 260 31 0.03 219 benign 0.218 25001 likely benign 25
1281 CCND1 rs779733976 SNP missense variant R/H 260 21 0.02 895 possibly damaging 0.894 31001 likely deleterious 31
1282 CCND1 rs749069429 SNP missense variant Q/P 261 41 0.04 52 benign 0.051 24001 likely benign 24
1283 CCND1 rs749069429 SNP missense variant Q/R 261 51 0.05 61 benign 0.06 24001 likely benign 24
1284 CCND1 rs1306960346 SNP missense variant Q/E 263 181 0.18 24 benign 0.023 21001 likely benign 21
1285 CCND1 rs768582800 SNP missense variant Q/K 264 71 0.07 45 benign 0.044 22001 likely benign 22
1286 CCND1 rs1225491115 SNP missense variant M/T 266 431 0.43 1 benign 0 13001 likely benign 13
1287 CCND1 rs377271027 SNP missense variant D/G 267 461 0.46 1 benign 0 21001 likely benign 21
1288 CCND1 rs1323012735 SNP missense variant P/T 268 81 0.08 66 benign 0.065 19001 likely benign 19
1289 CCND1 rs1252799046 SNP missense variant A/T 270 431 0.43 106 benign 0.105 20001 likely benign 20
1290 CCND1 rs770991095 SNP missense variant A/V 270 291 0.29 61 benign 0.06 17001 likely benign 17
1291 CCND1 rs759765773 SNP missense variant A/T 271 591 0.59 2 benign 0.001 4001 likely benign 4
1292 CCND1 rs759765773 SNP missense variant A/S 271 851 0.85 2 benign 0.001 1001 likely benign 1
1293 CCND1 rs770021448 SNP missense variant A/D 271 551 0.55 4 benign 0.003 14001 likely benign 14
1294 CCND1 rs775723921 SNP missense variant E/K 272 711 0.71 10 benign 0.009 22001 likely benign 22
1295 CCND1 rs764757265 SNP missense variant E/V 274 221 0.22 8 benign 0.007 22001 likely benign 22
1296 CCND1 rs752108957 SNP missense variant E/Q 275 451 0.45 28 benign 0.027 16001 likely benign 16
1297 CCND1 rs1436128793 SNP missense variant E/V 276 241 0.24 103 benign 0.102 22001 likely benign 22
1298 CCND1 rs200912411 SNP missense variant E/A 279 371 0.37 8 benign 0.007 21001 likely benign 21
1299 CCND1 rs749899296 SNP missense variant D/G 282 71 0.07 2 benign 0.001 23001 likely benign 23
1300 CCND1 rs749899296 SNP missense variant D/V 282 11 0.01 452 possibly damaging 0.451 25001 likely benign 25
1301 CCND1 rs755753468 SNP missense variant L/V 283 511 0.51 69 benign 0.068 18001 likely benign 18
1302 CCND1 rs754752470 SNP missense variant C/S 285 1001 1 2 benign 0.001 21001 likely benign 21
1303 CCND1 rs1168483993 SNP missense variant C/F 285 201 0.2 82 benign 0.081 23001 likely benign 23
1304 CCND1 rs771951669 SNP missense variant D/N 289 1 0 998 probably damaging 0.997 32001 likely deleterious 32
1305 CCND1 rs781165229 SNP missense variant D/E 289 21 0.02 999 probably damaging 0.998 23001 likely benign 23
1306 CCND1 rs769921935 SNP missense variant V/M 290 1 0 932 probably damaging 0.931 29001 likely benign 29
1307 CCND1 rs769921935 SNP missense variant V/L 290 21 0.02 902 possibly damaging 0.901 28001 likely benign 28
1308 CCND1 rs1292246537 SNP missense variant R/W 291 1 0 973 probably damaging 0.972 30001 likely deleterious 30
1309 CCND1 rs775768459 SNP missense variant R/Q 291 211 0.21 66 benign 0.065 23001 likely benign 23
1310 CCND1 rs775768459 SNP missense variant R/L 291 51 0.05 135 benign 0.134 24001 likely benign 24
1311 CCND1 rs535957987 SNP missense variant D/E 292 81 0.08 902 possibly damaging 0.901 8001 likely benign 8
1312 CCND1 rs1225090625 SNP missense variant V/M 293 1 0 909 possibly damaging 0.908 27001 likely benign 27
1313 PTEN rs1554900620 SNP missense variant L/P 2 1 0 1001 probably damaging 1 28001 likely benign 28
1314 PTEN rs1564837944 SNP missense variant H/R 5 461 0.46 1001 probably damaging 1 21001 likely benign 21
1315 PTEN rs1554900629 SNP missense variant K/Q 6 91 0.09 1001 probably damaging 1 24001 likely benign 24
1316 PTEN rs1554900633 SNP missense variant M/V 7 171 0.17 128 benign 0.127 22001 likely benign 22
1317 PTEN rs1554900635 SNP missense variant M/K 7 1 0 792 possibly damaging 0.791 24001 likely benign 24
1318 PTEN rs747072478 SNP missense variant M/I 7 1001 1 19 benign 0.018 22001 likely benign 22
1319 PTEN rs1434191423 SNP missense variant M/V 8 761 0.76 1 benign 0 21001 likely benign 21
1320 PTEN rs1434191423 SNP missense variant M/L 8 771 0.77 1 benign 0 22001 likely benign 22
1321 PTEN rs587781538 SNP missense variant M/K 8 481 0.48 38 benign 0.037 19001 likely benign 19
1322 PTEN rs587781538 SNP missense variant M/T 8 501 0.5 63 benign 0.062 20001 likely benign 20
1323 PTEN rs587782473 SNP missense variant F/V 9 21 0.02 904 possibly damaging 0.903 24001 likely benign 24
1324 PTEN rs786204867 SNP missense variant F/S 9 1 0 990 probably damaging 0.989 29001 likely benign 29
1325 PTEN rs786204944 SNP missense variant T/S 11 81 0.08 874 possibly damaging 0.873 22001 likely benign 22
1326 PTEN rs1085308053 SNP missense variant T/I 11 11 0.01 998 probably damaging 0.997 24001 likely benign 24
1327 PTEN rs1564837997 SNP missense variant I/V 12 651 0.65 8 benign 0.007 17001 likely benign 17
1328 PTEN rs786204868 SNP missense variant P/A 13 11 0.01 962 probably damaging 0.961 24001 likely benign 24
1329 PTEN rs786204868 SNP missense variant P/S 13 1 0 977 probably damaging 0.976 26001 likely benign 26
1330 PTEN rs776763121 SNP missense variant M/V 14 511 0.51 738 possibly damaging 0.737 20001 likely benign 20
1331 PTEN rs1185592373 SNP missense variant M/T 14 281 0.28 812 possibly damaging 0.811 21001 likely benign 21
1332 PTEN rs1554900653 SNP missense variant M/I 14 441 0.44 864 possibly damaging 0.863 22001 likely benign 22
1333 PTEN rs765433422 SNP missense variant G/R 18 51 0.05 169 benign 0.168 25001 likely benign 25
1334 PTEN rs1554900663 SNP missense variant T/A 19 21 0.02 486 possibly damaging 0.485 24001 likely benign 24
1335 PTEN rs121909232 SNP missense variant C/W 20 1 0 973 probably damaging 0.972 33001 likely deleterious 33
1336 PTEN rs1554825156 SNP missense variant N/S 21 801 0.8 198 benign 0.197 23001 likely benign 23
1337 PTEN rs1156887945 SNP missense variant P/H 22 1 0 995 probably damaging 0.994 26001 likely benign 26
1338 PTEN rs1564566726 SNP missense variant Q/P 23 201 0.2 603 possibly damaging 0.602 24001 likely benign 24
1339 PTEN rs121909234 SNP missense variant V/I 26 471 0.47 72 benign 0.071 22001 likely benign 22
1340 PTEN rs1060500117 SNP missense variant V/G 26 1 0 961 probably damaging 0.96 31001 likely deleterious 31
1341 PTEN rs1554825172 SNP missense variant Q/P 28 1 0 1000 probably damaging 0.999 28001 likely benign 28
1342 PTEN rs141373793 SNP missense variant L/P 29 111 0.11 995 probably damaging 0.994 25001 likely benign 25
1343 PTEN rs1221700050 SNP missense variant K/R 30 11 0.01 962 probably damaging 0.961 24001 likely benign 24
1344 PTEN rs878853943 SNP missense variant V/M 31 31 0.03 669 possibly damaging 0.668 25001 likely benign 25
1345 PTEN rs878853943 SNP missense variant V/L 31 21 0.02 669 possibly damaging 0.668 25001 likely benign 25
1346 PTEN rs778528056 SNP missense variant K/R 32 101 0.1 948 probably damaging 0.947 26001 likely benign 26
1347 PTEN rs778528056 SNP missense variant K/M 32 1 0 993 probably damaging 0.992 33001 likely deleterious 33
1348 PTEN rs1554825177 SNP missense variant I/L 33 331 0.33 998 probably damaging 0.997 23001 likely benign 23
1349 PTEN rs786204946 SNP missense variant I/M 33 11 0.01 1001 probably damaging 1 22001 likely benign 22
1350 PTEN rs876659433 SNP missense variant Y/H 34 861 0.86 2 benign 0.001 22001 likely benign 22
1351 PTEN rs905615413 SNP missense variant S/F 36 1 0 829 possibly damaging 0.828 27001 likely benign 27
1352 PTEN rs748240670 SNP missense variant N/S 37 401 0.4 8 benign 0.007 8001 likely benign 8
1353 PTEN rs587781998 SNP missense variant S/T 38 661 0.66 8 benign 0.007 20001 likely benign 20
1354 PTEN rs1214965807 SNP missense variant S/L 38 611 0.61 8 benign 0.007 23001 likely benign 23
1355 PTEN rs1554825190 SNP missense variant P/L 40 751 0.75 6 benign 0.005 22001 likely benign 22
1356 PTEN rs770025422 SNP missense variant R/Q 42 21 0.02 560 possibly damaging 0.559 23001 likely benign 23
1357 PTEN rs786201730 SNP missense variant R/G 43 191 0.19 701 possibly damaging 0.7 24001 likely benign 24
1358 PTEN rs786201730 SNP missense variant R/W 43 121 0.12 140 benign 0.139 26001 likely benign 26
1359 PTEN rs121909235 SNP missense variant R/Q 43 161 0.16 756 possibly damaging 0.755 25001 likely benign 25
1360 PTEN rs786201758 SNP missense variant M/V 48 601 0.6 8 benign 0.007 21001 likely benign 21
1361 PTEN rs786204871 SNP missense variant M/T 48 291 0.29 31 benign 0.03 22001 likely benign 22
1362 PTEN rs786204871 SNP missense variant M/R 48 11 0.01 727 possibly damaging 0.726 26001 likely benign 26
1363 PTEN rs1554825207 SNP missense variant F/L 50 301 0.3 390 benign 0.389 16001 likely benign 16
1364 PTEN rs1554825207 SNP missense variant F/V 50 171 0.17 78 benign 0.077 23001 likely benign 23
1365 PTEN rs121909240 SNP missense variant F/S 50 71 0.07 112 benign 0.111 23001 likely benign 23
1366 PTEN rs17849090 SNP missense variant F/L 50 301 0.3 390 benign 0.389 16001 likely benign 16
1367 PTEN rs1064794675 SNP missense variant P/S 53 161 0.16 992 probably damaging 0.991 23001 likely benign 23
1368 PTEN rs1057518538 SNP missense variant Q/P 54 61 0.06 957 probably damaging 0.956 23001 likely benign 23
1369 PTEN rs587782350 SNP missense variant P/L 55 51 0.05 21 benign 0.02 23001 likely benign 23
1370 PTEN rs1057519368 SNP missense variant L/S 56 1 0 1001 probably damaging 1 29001 likely benign 29
1371 PTEN rs1564566931 SNP missense variant P/S 57 11 0.01 1001 probably damaging 1 24001 likely benign 24
1372 PTEN rs759560822 SNP missense variant P/R 57 1 0 1001 probably damaging 1 26001 likely benign 26
1373 PTEN rs1114167664 substitution missense variant G/V 60 1 0 993 probably damaging 0.992 29001 likely benign 29
1374 PTEN rs1554825226 SNP missense variant G/A 60 11 0.01 982 probably damaging 0.981 27001 likely benign 27
1375 PTEN rs1554825226 SNP missense variant G/V 60 1 0 993 probably damaging 0.992 29001 likely benign 29
1376 PTEN rs121909239 SNP missense variant D/G 61 11 0.01 991 probably damaging 0.99 29001 likely benign 29
1377 PTEN rs121909239 SNP missense variant D/V 61 1 0 994 probably damaging 0.993 29001 likely benign 29
1378 PTEN rs1554825235 SNP missense variant I/N 62 1 0 980 probably damaging 0.979 29001 likely benign 29
1379 PTEN rs1114167633 SNP missense variant K/T 63 1 0 1001 probably damaging 1 28001 likely benign 28
1380 PTEN rs1564566998 SNP missense variant V/E 64 1 0 888 possibly damaging 0.887 28001 likely benign 28
1381 PTEN rs1554825245 SNP missense variant F/L 66 51 0.05 840 possibly damaging 0.839 22001 likely benign 22
1382 PTEN rs1060500125 SNP missense variant K/R 69 41 0.04 107 benign 0.106 24001 likely benign 24
1383 PTEN rs760146269 SNP missense variant Q/H 70 161 0.16 915 probably damaging 0.914 24001 likely benign 24
1384 PTEN rs763784377 SNP missense variant N/T 71 51 0.05 544 possibly damaging 0.543 23001 likely benign 23
1385 PTEN rs763784377 SNP missense variant N/S 71 161 0.16 69 benign 0.068 22001 likely benign 22
1386 PTEN rs786204872 SNP missense variant L/V 74 231 0.23 136 benign 0.135 20001 likely benign 20
1387 PTEN rs1335033900 SNP missense variant L/P 74 161 0.16 714 possibly damaging 0.713 25001 likely benign 25
1388 PTEN rs1335033900 SNP missense variant L/R 74 271 0.27 482 possibly damaging 0.481 23001 likely benign 23
1389 PTEN rs1554825264 SNP missense variant K/R 76 151 0.15 842 possibly damaging 0.841 25001 likely benign 25
1390 PTEN rs1554825266 SNP missense variant K/N 76 1 0 926 probably damaging 0.925 35001 likely deleterious 35
1391 PTEN rs398123328 SNP missense variant D/E 77 1001 1 45 benign 0.044 12001 likely benign 12
1392 PTEN rs1554825502 SNP missense variant M/V 79 41 0.04 299 benign 0.298 22001 likely benign 22
1393 PTEN rs1195369834 SNP missense variant M/I 79 11 0.01 278 benign 0.277 23001 likely benign 23
1394 PTEN rs142420551 SNP missense variant F/S 80 1 0 981 probably damaging 0.98 32001 likely deleterious 32
1395 PTEN rs1114167648 SNP missense variant H/P 81 11 0.01 938 probably damaging 0.937 27001 likely benign 27
1396 PTEN rs786204875 SNP missense variant W/L 83 1 0 1001 probably damaging 1 32001 likely deleterious 32
1397 PTEN rs1410198544 SNP missense variant V/I 84 591 0.59 95 benign 0.094 21001 likely benign 21
1398 PTEN rs1564568216 SNP missense variant T/A 86 11 0.01 493 possibly damaging 0.492 26001 likely benign 26
1399 PTEN rs398123329 SNP missense variant T/K 86 1 0 390 benign 0.389 26001 likely benign 26
1400 PTEN rs398123329 SNP missense variant T/R 86 1 0 827 possibly damaging 0.826 25001 likely benign 25
1401 PTEN rs398123329 SNP missense variant T/I 86 31 0.03 106 benign 0.105 23001 likely benign 23
1402 PTEN rs867171992 SNP missense variant F/L 87 1 0 604 possibly damaging 0.603 24001 likely benign 24
1403 PTEN rs1474354667 SNP missense variant I/V 89 591 0.59 160 benign 0.159 18001 likely benign 18
1404 PTEN rs750705904 SNP missense variant P/A 90 351 0.35 934 probably damaging 0.933 23001 likely benign 23
1405 PTEN rs750705904 SNP missense variant P/S 90 311 0.31 934 probably damaging 0.933 23001 likely benign 23
1406 PTEN rs876658988 SNP missense variant P/A 92 411 0.41 611 possibly damaging 0.61 19001 likely benign 19
1407 PTEN rs876658988 SNP missense variant P/S 92 431 0.43 169 benign 0.168 19001 likely benign 19
1408 PTEN rs1564568265 SNP missense variant E/K 94 301 0.3 161 benign 0.16 24001 likely benign 24
1409 PTEN rs1554825526 SNP missense variant S/P 96 411 0.41 4 benign 0.003 22001 likely benign 22
1410 PTEN rs1554825528 SNP missense variant E/K 97 201 0.2 183 benign 0.182 23001 likely benign 23
1411 PTEN rs562015640 SNP missense variant K/E 98 361 0.36 60 benign 0.059 22001 likely benign 22
1412 PTEN rs35600253 SNP missense variant V/L 99 541 0.54 19 benign 0.018 21001 likely benign 21
1413 PTEN rs876661234 SNP missense variant V/A 99 281 0.28 143 benign 0.142 22001 likely benign 22
1414 PTEN rs1564568318 SNP missense variant E/G 100 141 0.14 1001 probably damaging 1 25001 likely benign 25
1415 PTEN rs1175543698 SNP missense variant S/N 103 321 0.32 463 possibly damaging 0.462 22001 likely benign 22
1416 PTEN rs143335584 SNP missense variant S/R 103 71 0.07 806 possibly damaging 0.805 23001 likely benign 23
1417 PTEN rs786202207 SNP missense variant C/R 105 371 0.37 114 benign 0.113 21001 likely benign 21
1418 PTEN rs1060500121 SNP missense variant C/Y 105 901 0.9 92 benign 0.091 19001 likely benign 19
1419 PTEN rs370064195 SNP missense variant D/H 106 161 0.16 643 possibly damaging 0.642 25001 likely benign 25
1420 PTEN rs370064195 SNP missense variant D/Y 106 11 0.01 623 possibly damaging 0.622 24001 likely benign 24
1421 PTEN rs371387815 SNP missense variant Q/K 107 661 0.66 1 benign 0 16001 likely benign 16
1422 PTEN rs371387815 SNP missense variant Q/E 107 801 0.8 40 benign 0.039 15001 likely benign 15
1423 PTEN rs1554825550 SNP missense variant E/G 108 261 0.26 31 benign 0.03 23001 likely benign 23
1424 PTEN rs758644748 SNP missense variant D/N 110 471 0.47 376 benign 0.375 22001 likely benign 22
1425 PTEN rs1334444415 SNP missense variant S/G 111 181 0.18 1 benign 0 21001 likely benign 21
1426 PTEN rs745638189 SNP missense variant S/N 111 131 0.13 8 benign 0.007 21001 likely benign 21
1427 PTEN rs876660906 SNP missense variant S/R 111 101 0.1 256 benign 0.255 17001 likely benign 17
1428 PTEN rs1114167660 SNP missense variant I/V 112 701 0.7 8 benign 0.007 18001 likely benign 18
1429 PTEN rs772018727 SNP missense variant I/S 112 561 0.56 150 benign 0.149 22001 likely benign 22
1430 PTEN rs775461980 SNP missense variant S/G 114 121 0.12 8 benign 0.007 22001 likely benign 22
1431 PTEN rs587780007 SNP missense variant S/N 114 201 0.2 20 benign 0.019 22001 likely benign 22
1432 PTEN rs587780007 SNP missense variant S/I 114 21 0.02 137 benign 0.136 24001 likely benign 24
1433 PTEN rs876658345 SNP missense variant S/R 114 111 0.11 20 benign 0.019 21001 likely benign 21
1434 PTEN rs786203858 SNP missense variant I/V 115 591 0.59 1 benign 0 19001 likely benign 19
1435 PTEN rs746930141 SNP missense variant E/Q 116 391 0.39 50 benign 0.049 22001 likely benign 22
1436 PTEN rs1197734477 SNP missense variant E/G 116 301 0.3 13 benign 0.012 22001 likely benign 22
1437 PTEN rs1064794436 SNP missense variant R/C 117 121 0.12 6 benign 0.005 23001 likely benign 23
1438 PTEN rs786201507 SNP missense variant R/H 117 161 0.16 6 benign 0.005 23001 likely benign 23
1439 PTEN rs1564568473 SNP missense variant D/G 119 111 0.11 31 benign 0.03 24001 likely benign 24
1440 PTEN rs878853946 SNP missense variant D/N 121 131 0.13 895 possibly damaging 0.894 23001 likely benign 23
1441 PTEN rs863224667 SNP missense variant D/G 121 271 0.27 161 benign 0.16 23001 likely benign 23
1442 PTEN rs562164491 SNP missense variant K/N 122 141 0.14 878 possibly damaging 0.877 18001 likely benign 18
1443 PTEN rs1171478249 SNP missense variant E/A 123 201 0.2 694 possibly damaging 0.693 23001 likely benign 23
1444 PTEN rs1554825577 SNP missense variant L/I 125 71 0.07 967 probably damaging 0.966 22001 likely benign 22
1445 PTEN rs1064793345 SNP missense variant L/P 125 11 0.01 1000 probably damaging 0.999 25001 likely benign 25
1446 PTEN rs876658630 SNP missense variant V/I 126 601 0.6 2 benign 0.001 19001 likely benign 19
1447 PTEN rs761350690 SNP missense variant T/N 128 71 0.07 482 possibly damaging 0.481 23001 likely benign 23
1448 PTEN rs761350690 SNP missense variant T/I 128 151 0.15 30 benign 0.029 23001 likely benign 23
1449 PTEN rs1373782343 SNP missense variant D/Y 133 11 0.01 968 probably damaging 0.967 29001 likely benign 29
1450 PTEN rs1114167654 SNP missense variant L/P 134 1 0 995 probably damaging 0.994 28001 likely benign 28
1451 PTEN rs1114167654 SNP missense variant L/R 134 1 0 520 possibly damaging 0.519 24001 likely benign 24
1452 PTEN rs1554825607 SNP missense variant K/E 139 1 0 858 possibly damaging 0.857 27001 likely benign 27
1453 PTEN rs1554825616 SNP missense variant A/V 142 91 0.09 953 probably damaging 0.952 24001 likely benign 24
1454 PTEN rs1206321984 SNP missense variant N/S 143 21 0.02 1000 probably damaging 0.999 25001 likely benign 25
1455 PTEN rs1554825620 SNP missense variant N/K 143 61 0.06 1000 probably damaging 0.999 22001 likely benign 22
1456 PTEN rs1085308040 SNP missense variant R/Q 144 61 0.06 264 benign 0.263 24001 likely benign 24
1457 PTEN rs1085308040 SNP missense variant R/L 144 51 0.05 873 possibly damaging 0.872 25001 likely benign 25
1458 PTEN rs1554825641 SNP missense variant F/Y 146 281 0.28 937 probably damaging 0.936 24001 likely benign 24
1459 PTEN rs1564568679 SNP missense variant P/Q 148 1 0 1001 probably damaging 1 24001 likely benign 24
1460 PTEN rs759852661 SNP missense variant N/H 149 11 0.01 1001 probably damaging 1 26001 likely benign 26
1461 PTEN rs759852661 SNP missense variant N/D 149 261 0.26 1000 probably damaging 0.999 23001 likely benign 23
1462 PTEN rs1554825649 SNP missense variant N/K 149 11 0.01 1000 probably damaging 0.999 25001 likely benign 25
1463 PTEN rs1554825652 SNP missense variant F/V 150 1 0 1000 probably damaging 0.999 28001 likely benign 28
1464 PTEN rs1064794080 SNP missense variant K/T 151 1 0 962 probably damaging 0.961 33001 likely deleterious 33
1465 PTEN rs398123314 SNP missense variant K/N 151 21 0.02 948 probably damaging 0.947 35001 likely deleterious 35
1466 PTEN rs786201041 SNP missense variant V/I 152 1 0 982 probably damaging 0.981 34001 likely deleterious 34
1467 PTEN rs786201041 SNP missense variant V/L 152 1 0 944 probably damaging 0.943 34001 likely deleterious 34
1468 PTEN rs1114167624 SNP missense variant V/A 152 1 0 986 probably damaging 0.985 32001 likely deleterious 32
1469 PTEN rs1114167624 SNP missense variant V/G 152 1 0 998 probably damaging 0.997 34001 likely deleterious 34
1470 PTEN rs1274425509 SNP missense variant S/R 153 21 0.02 19 benign 0.018 23001 likely benign 23
1471 ERBB2 rs1379316719 SNP missense variant E/G 2 11 0.01 1 benign 0 26001 likely benign 26
1472 ERBB2 rs1039589946 SNP missense variant A/S 4 141 0.14 2 benign 0.001 22001 likely benign 22
1473 ERBB2 rs1428243929 SNP missense variant A/V 4 11 0.01 52 benign 0.051 23001 likely benign 23
1474 ERBB2 rs1456994901 SNP missense variant L/F 11 301 0.3 1 benign 0 17001 likely benign 17
1475 ERBB2 rs1318994039 SNP missense variant L/F 12 71 0.07 970 probably damaging 0.969 23001 likely benign 23
1476 ERBB2 rs1263781765 SNP missense variant L/F 13 161 0.16 1 benign 0 17001 likely benign 17
1477 ERBB2 rs1442246817 SNP missense variant A/S 14 681 0.68 210 benign 0.209 17001 likely benign 17
1478 ERBB2 rs1293505485 SNP missense variant A/V 14 311 0.31 2 benign 0.001 21001 likely benign 21
1479 ERBB2 rs193171026 SNP missense variant L/F 15 81 0.08 541 possibly damaging 0.54 23001 likely benign 23
1480 ERBB2 rs1225599701 SNP missense variant L/V 16 421 0.42 900 possibly damaging 0.899 21001 likely benign 21
1481 ERBB2 rs1567892325 SNP missense variant L/F 16 221 0.22 970 probably damaging 0.969 23001 likely benign 23
1482 ERBB2 rs1307888184 SNP missense variant P/T 17 411 0.41 18 benign 0.017 15001 likely benign 15
1483 ERBB2 rs1307888184 SNP missense variant P/S 17 441 0.44 1 benign 0 15001 likely benign 15
1484 ERBB2 rs1184958761 SNP missense variant P/S 18 431 0.43 1 benign 0 17001 likely benign 17
1485 ERBB2 rs1486972911 SNP missense variant G/R 19 61 0.06 4 benign 0.003 22001 likely benign 22
1486 ERBB2 rs993479758 SNP missense variant G/A 19 281 0.28 2 benign 0.001 19001 likely benign 19
1487 ERBB2 rs1004896536 SNP missense variant A/V 21 611 0.61 30 benign 0.029 18001 likely benign 18
1488 ERBB2 rs896376245 SNP missense variant S/N 22 421 0.42 1 benign 0 19001 likely benign 19
1489 ERBB2 rs755921683 SNP missense variant V/A 25 31 0.03 75 benign 0.074 15001 likely benign 15
1490 ERBB2 rs779913120 SNP missense variant T/P 27 331 0.33 557 possibly damaging 0.556 23001 likely benign 23
1491 ERBB2 rs1365546088 SNP missense variant T/I 27 251 0.25 260 benign 0.259 20001 likely benign 20
1492 ERBB2 rs564064363 SNP missense variant G/S 28 1 0 1000 probably damaging 0.999 29001 likely benign 29
1493 ERBB2 rs564064363 SNP missense variant G/R 28 1 0 1001 probably damaging 1 29001 likely benign 29
1494 ERBB2 rs1284110310 SNP missense variant G/D 28 1 0 1001 probably damaging 1 27001 likely benign 27
1495 ERBB2 rs778487069 SNP missense variant D/Y 30 11 0.01 853 possibly damaging 0.852 28001 likely benign 28
1496 ERBB2 rs998740859 SNP missense variant M/L 31 51 0.05 4 benign 0.003 22001 likely benign 22
1497 ERBB2 rs546886845 SNP missense variant M/I 31 21 0.02 62 benign 0.061 24001 likely benign 24
1498 ERBB2 rs149937802 SNP missense variant R/W 34 11 0.01 467 possibly damaging 0.466 25001 likely benign 25
1499 ERBB2 rs921911454 SNP missense variant R/Q 34 311 0.31 1 benign 0 13001 likely benign 13
1500 ERBB2 rs777171280 SNP missense variant L/P 35 121 0.12 12 benign 0.011 15001 likely benign 15
1501 ERBB2 rs765607521 SNP missense variant A/P 37 101 0.1 99 benign 0.098 21001 likely benign 21
1502 ERBB2 rs1459247021 SNP missense variant S/G 38 21 0.02 807 possibly damaging 0.806 25001 likely benign 25
1503 ERBB2 rs1216236852 SNP missense variant P/A 39 501 0.5 4 benign 0.003 16001 likely benign 16
1504 ERBB2 rs763193414 SNP missense variant E/K 40 21 0.02 627 possibly damaging 0.626 26001 likely benign 26
1505 ERBB2 rs1311415529 SNP missense variant D/V 44 241 0.24 4 benign 0.003 22001 likely benign 22
1506 ERBB2 rs587778266 SNP missense variant M/V 45 81 0.08 2 benign 0.001 19001 likely benign 19
1507 ERBB2 rs1281942958 SNP missense variant M/I 45 11 0.01 2 benign 0.001 22001 likely benign 22
1508 ERBB2 rs764222200 SNP missense variant L/P 46 1 0 935 probably damaging 0.934 28001 likely benign 28
1509 ERBB2 rs1236052395 SNP missense variant R/C 47 11 0.01 438 benign 0.437 23001 likely benign 23
1510 ERBB2 rs144019910 SNP missense variant R/H 47 71 0.07 1 benign 0 22001 likely benign 22
1511 ERBB2 rs1187611727 SNP missense variant L/F 49 51 0.05 852 possibly damaging 0.851 23001 likely benign 23
1512 ERBB2 rs1390107974 SNP missense variant Q/R 51 231 0.23 1 benign 0 20001 likely benign 20
1513 ERBB2 rs1220384939 SNP missense variant Q/H 51 41 0.04 1 benign 0 21001 likely benign 21
1514 ERBB2 rs140441229 SNP missense variant Q/R 57 21 0.02 856 possibly damaging 0.855 26001 likely benign 26
1515 ERBB2 rs1298421770 SNP missense variant G/E 58 291 0.29 913 probably damaging 0.912 24001 likely benign 24
1516 ERBB2 rs1332501526 SNP missense variant L/V 60 1 0 1001 probably damaging 1 23001 likely benign 23
1517 ERBB2 rs766186178 SNP missense variant E/Q 61 1 0 1001 probably damaging 1 27001 likely benign 27
1518 ERBB2 rs1013215187 SNP missense variant L/V 62 101 0.1 49 benign 0.048 21001 likely benign 21
1519 ERBB2 rs753655456 SNP missense variant T/I 63 1 0 1001 probably damaging 1 25001 likely benign 25
1520 ERBB2 rs1364385133 SNP missense variant P/L 66 281 0.28 38 benign 0.037 19001 likely benign 19
1521 ERBB2 rs778575008 SNP missense variant T/A 67 751 0.75 1 benign 0 14001 likely benign 14
1522 ERBB2 rs752339377 SNP missense variant T/I 67 151 0.15 42 benign 0.041 19001 likely benign 19
1523 ERBB2 rs757899978 SNP missense variant N/S 68 181 0.18 4 benign 0.003 15001 likely benign 15
1524 ERBB2 rs777347427 SNP missense variant A/G 69 311 0.31 183 benign 0.182 22001 likely benign 22
1525 ERBB2 rs61737968 SNP missense variant E/A 79 1 0 1001 probably damaging 1 28001 likely benign 28
1526 ERBB2 rs376524324 SNP missense variant V/M 84 11 0.01 655 possibly damaging 0.654 23001 likely benign 23
1527 ERBB2 rs759478535 SNP missense variant I/V 86 401 0.4 32 benign 0.031 18001 likely benign 18
1528 ERBB2 rs775382058 SNP missense variant A/T 87 1 0 999 probably damaging 0.998 29001 likely benign 29
1529 ERBB2 rs1181714248 SNP missense variant H/Y 88 211 0.21 324 benign 0.323 19001 likely benign 19
1530 ERBB2 rs762638680 SNP missense variant H/Q 88 401 0.4 7 benign 0.006 16001 likely benign 16
1531 ERBB2 rs763850846 SNP missense variant Q/P 90 171 0.17 217 benign 0.216 9001 likely benign 9
1532 ERBB2 rs1368945502 SNP missense variant Q/R 93 391 0.39 1 benign 0 10001 likely benign 10
1533 ERBB2 rs767151455 SNP missense variant P/L 95 1 0 991 probably damaging 0.99 25001 likely benign 25
1534 ERBB2 rs749886389 SNP missense variant R/W 100 1 0 1000 probably damaging 0.999 24001 likely benign 24
1535 ERBB2 rs756720659 SNP missense variant R/Q 100 321 0.32 342 benign 0.341 23001 likely benign 23
1536 ERBB2 rs539140755 SNP missense variant I/T 101 1 0 995 probably damaging 0.994 27001 likely benign 27
1537 ERBB2 rs950730453 SNP missense variant R/Q 103 1 0 1001 probably damaging 1 31001 likely deleterious 31
1538 ERBB2 rs1348253156 SNP missense variant T/I 105 51 0.05 896 possibly damaging 0.895 23001 likely benign 23
1539 ERBB2 rs1395467940 SNP missense variant Q/E 106 671 0.67 534 possibly damaging 0.533 22001 likely benign 22
1540 ERBB2 rs1416951791 SNP missense variant Q/H 106 121 0.12 926 probably damaging 0.925 23001 likely benign 23
1541 ERBB2 rs749711404 SNP missense variant D/G 110 671 0.67 4 benign 0.003 22001 likely benign 22
1542 ERBB2 rs749711404 SNP missense variant D/V 110 11 0.01 322 benign 0.321 24001 likely benign 24
1543 ERBB2 rs1340287026 SNP missense variant N/S 111 631 0.63 1 benign 0 1 likely benign 0
1544 ERBB2 rs1253654469 SNP missense variant Y/C 112 1 0 985 probably damaging 0.984 24001 likely benign 24
1545 ERBB2 rs1272695341 SNP missense variant A/T 115 91 0.09 258 benign 0.257 23001 likely benign 23
1546 ERBB2 rs748301823 SNP missense variant A/V 115 51 0.05 36 benign 0.035 22001 likely benign 22
1547 ERBB2 rs1256572460 SNP missense variant V/M 116 1 0 993 probably damaging 0.992 27001 likely benign 27
1548 ERBB2 rs1423090731 SNP missense variant V/A 116 41 0.04 859 possibly damaging 0.858 26001 likely benign 26
1549 ERBB2 rs769775277 SNP missense variant D/N 121 501 0.5 7 benign 0.006 19001 likely benign 19
1550 ERBB2 rs141135746 SNP missense variant P/A 122 741 0.74 1 benign 0 7001 likely benign 7
1551 ERBB2 rs370959592 SNP missense variant P/L 122 351 0.35 1 benign 0 6001 likely benign 6
1552 ERBB2 rs1283546661 SNP missense variant N/Y 124 141 0.14 291 benign 0.29 17001 likely benign 17
1553 ERBB2 rs970583285 SNP missense variant T/P 127 131 0.13 13 benign 0.012 11001 likely benign 11
1554 ERBB2 rs761564667 SNP missense variant P/A 128 371 0.37 1 benign 0 1001 likely benign 1
1555 ERBB2 rs373824622 SNP missense variant P/R 128 231 0.23 125 benign 0.124 12001 likely benign 12
1556 ERBB2 rs766949725 SNP missense variant V/F 129 681 0.68 79 benign 0.078 11001 likely benign 11
1557 ERBB2 rs754295165 SNP missense variant P/S 134 781 0.78 4 benign 0.003 8001 likely benign 8
1558 ERBB2 rs865925114 SNP missense variant P/Q 134 601 0.6 4 benign 0.003 11001 likely benign 11
1559 ERBB2 rs755427616 SNP missense variant G/S 136 1 0 996 probably damaging 0.995 27001 likely benign 27
1560 ERBB2 rs200208742 SNP missense variant L/Q 137 1 0 998 probably damaging 0.997 27001 likely benign 27
1561 ERBB2 rs200208742 SNP missense variant L/P 137 1 0 1000 probably damaging 0.999 28001 likely benign 28
1562 ERBB2 rs200208742 SNP missense variant L/R 137 1 0 947 probably damaging 0.946 27001 likely benign 27
1563 ERBB2 rs779156384 SNP missense variant R/W 138 1 0 929 probably damaging 0.928 26001 likely benign 26
1564 ERBB2 rs748476466 SNP missense variant R/Q 138 191 0.19 59 benign 0.058 15001 likely benign 15
1565 ERBB2 rs758646541 SNP missense variant E/D 139 11 0.01 768 possibly damaging 0.767 24001 likely benign 24
1566 ERBB2 rs1304310205 SNP missense variant L/V 142 1 0 570 possibly damaging 0.569 28001 likely benign 28
1567 ERBB2 rs185670819 SNP missense variant R/Q 143 61 0.06 83 benign 0.082 22001 likely benign 22
1568 ERBB2 rs185670819 SNP missense variant R/P 143 11 0.01 907 possibly damaging 0.906 26001 likely benign 26
1569 ERBB2 rs1187893378 SNP missense variant S/N 144 841 0.84 4 benign 0.003 17001 likely benign 17
1570 ERBB2 rs527779103 SNP missense variant L/F 145 1 0 1000 probably damaging 0.999 26001 likely benign 26
1571 ERBB2 rs200963868 SNP missense variant G/V 151 1 0 1001 probably damaging 1 32001 likely deleterious 32
1572 ERBB2 rs151122410 SNP missense variant G/A 152 181 0.18 265 benign 0.264 22001 likely benign 22
1573 ERBB2 rs778041266 SNP missense variant V/L 153 31 0.03 507 possibly damaging 0.506 24001 likely benign 24
1574 ERBB2 rs757446217 SNP missense variant L/F 154 651 0.65 14 benign 0.013 19001 likely benign 19
1575 ERBB2 rs781137961 SNP missense variant R/W 157 21 0.02 777 possibly damaging 0.776 27001 likely benign 27
1576 ERBB2 rs745921471 SNP missense variant R/Q 157 771 0.77 13 benign 0.012 22001 likely benign 22
1577 ERBB2 rs768502081 SNP missense variant N/K 158 1 0 965 probably damaging 0.964 24001 likely benign 24
1578 ERBB2 rs778888794 SNP missense variant P/T 159 81 0.08 568 possibly damaging 0.567 22001 likely benign 22
1579 ERBB2 rs778888794 SNP missense variant P/S 159 11 0.01 887 possibly damaging 0.886 24001 likely benign 24
1580 ERBB2 rs1474799396 SNP missense variant P/L 159 31 0.03 952 probably damaging 0.951 25001 likely benign 25
1581 ERBB2 rs1327422858 SNP missense variant Q/L 160 651 0.65 100 benign 0.099 22001 likely benign 22
1582 ERBB2 rs774604250 SNP missense variant L/V 161 1 0 994 probably damaging 0.993 24001 likely benign 24
1583 ERBB2 rs1567899208 SNP missense variant Y/C 163 161 0.16 871 possibly damaging 0.87 23001 likely benign 23
1584 ERBB2 rs747995543 SNP missense variant Q/R 164 101 0.1 987 probably damaging 0.986 23001 likely benign 23
1585 ERBB2 rs771986239 SNP missense variant D/H 165 31 0.03 183 benign 0.182 24001 likely benign 24
1586 ERBB2 rs1227559137 SNP missense variant T/M 166 21 0.02 389 benign 0.388 15001 likely benign 15
1587 ERBB2 rs1269105876 SNP missense variant K/Q 170 961 0.96 1 benign 0 5001 likely benign 5
1588 ERBB2 rs1269105876 SNP missense variant K/E 170 951 0.95 1 benign 0 6001 likely benign 6
1589 ERBB2 rs1222267645 SNP missense variant K/T 175 271 0.27 10 benign 0.009 19001 likely benign 19
1590 ERBB2 rs1222267645 SNP missense variant K/R 175 191 0.19 2 benign 0.001 19001 likely benign 19
1591 ERBB2 rs776032539 SNP missense variant N/S 177 541 0.54 1 benign 0 16001 likely benign 16
1592 ERBB2 rs1053130436 SNP missense variant Q/K 178 951 0.95 1 benign 0 5001 likely benign 5
1593 ERBB2 rs1053130436 SNP missense variant Q/E 178 1001 1 1 benign 0 3001 likely benign 3
1594 ERBB2 rs1010848650 SNP missense variant L/V 183 511 0.51 1 benign 0 1 likely benign 0
1595 ERBB2 rs1416532705 SNP missense variant T/I 186 171 0.17 11 benign 0.01 7001 likely benign 7
1596 ERBB2 rs765706190 SNP missense variant R/S 188 911 0.91 13 benign 0.012 15001 likely benign 15
1597 ERBB2 rs765706190 SNP missense variant R/C 188 91 0.09 755 possibly damaging 0.754 23001 likely benign 23
1598 ERBB2 rs763371007 SNP missense variant R/H 188 391 0.39 2 benign 0.001 17001 likely benign 17
1599 ERBB2 rs753419830 SNP missense variant R/W 190 21 0.02 926 probably damaging 0.925 23001 likely benign 23
1600 ERBB2 rs531563820 SNP missense variant R/Q 190 581 0.58 433 benign 0.432 20001 likely benign 20
1601 ERBB2 rs531563820 SNP missense variant R/P 190 361 0.36 31 benign 0.03 19001 likely benign 19
1602 ERBB2 rs769335702 SNP missense variant H/Q 193 1001 1 1 benign 0 1 likely benign 0
1603 ERBB2 rs763458661 SNP missense variant P/S 194 241 0.24 16 benign 0.015 14001 likely benign 14
1604 ERBB2 rs764545872 SNP missense variant P/L 194 81 0.08 13 benign 0.012 16001 likely benign 16
1605 ERBB2 rs1209871684 SNP missense variant C/Y 195 1 0 994 probably damaging 0.993 24001 likely benign 24
1606 ERBB2 rs1241783659 SNP missense variant S/F 196 41 0.04 461 possibly damaging 0.46 22001 likely benign 22
1607 ERBB2 rs113619125 SNP missense variant P/L 197 31 0.03 128 benign 0.127 17001 likely benign 17
1608 ERBB2 rs1451675784 SNP missense variant M/L 198 201 0.2 1 benign 0 6001 likely benign 6
1609 ERBB2 rs908142099 SNP missense variant M/T 198 131 0.13 1 benign 0 2001 likely benign 2
1610 ERBB2 rs767673890 SNP missense variant M/I 198 81 0.08 1 benign 0 2001 likely benign 2
1611 ERBB2 rs750651941 SNP missense variant G/V 201 161 0.16 4 benign 0.003 1 likely benign 0
1612 ERBB2 rs1185455152 SNP missense variant S/P 202 121 0.12 1 benign 0 3001 likely benign 3
1613 ERBB2 rs1426154971 SNP missense variant S/F 202 1 0 394 benign 0.393 18001 likely benign 18
1614 ERBB2 rs971655376 SNP missense variant R/C 203 171 0.17 128 benign 0.127 11001 likely benign 11
1615 ERBB2 rs896171398 SNP missense variant R/H 203 721 0.72 1 benign 0 4001 likely benign 4
1616 ERBB2 rs896171398 SNP missense variant R/P 203 211 0.21 48 benign 0.047 9001 likely benign 9
1617 ERBB2 rs1265935073 SNP missense variant D/Y 211 191 0.19 30 benign 0.029 24001 likely benign 24
1618 ERBB2 rs1363819722 SNP missense variant C/W 212 1 0 1001 probably damaging 1 25001 likely benign 25
1619 ERBB2 rs753902254 SNP missense variant S/I 214 201 0.2 2 benign 0.001 6001 likely benign 6
1620 ERBB2 rs770976272 SNP missense variant T/M 216 1 0 1001 probably damaging 1 25001 likely benign 25
1621 ERBB2 rs768151310 SNP missense variant R/C 217 1 0 917 probably damaging 0.916 23001 likely benign 23
1622 ERBB2 rs779346332 SNP missense variant R/H 217 51 0.05 34 benign 0.033 21001 likely benign 21
1623 ERBB2 rs1473418882 SNP missense variant T/A 218 381 0.38 8 benign 0.007 18001 likely benign 18
1624 ERBB2 rs1182661036 SNP missense variant T/I 218 461 0.46 58 benign 0.057 14001 likely benign 14
1625 ERBB2 rs1004581055 SNP missense variant V/L 219 541 0.54 1 benign 0 3001 likely benign 3
1626 ERBB2 rs772393268 SNP missense variant G/S 222 601 0.6 2 benign 0.001 3001 likely benign 3
1627 ERBB2 rs1164981758 SNP missense variant G/D 222 101 0.1 67 benign 0.066 16001 likely benign 16
1628 ERBB2 rs1308425150 SNP missense variant G/S 223 171 0.17 118 benign 0.117 23001 likely benign 23
1629 ERBB2 rs1390819673 SNP missense variant G/D 223 181 0.18 646 possibly damaging 0.645 24001 likely benign 24
1630 ERBB2 rs1404246175 SNP missense variant A/V 225 51 0.05 118 benign 0.117 22001 likely benign 22
1631 ERBB2 rs760895559 SNP missense variant R/C 226 1 0 1001 probably damaging 1 28001 likely benign 28
1632 ERBB2 rs745625627 SNP missense variant R/H 226 1 0 1000 probably damaging 0.999 31001 likely deleterious 31
1633 ERBB2 rs981689859 SNP missense variant G/R 229 11 0.01 998 probably damaging 0.997 29001 likely benign 29
1634 ERBB2 rs776960538 SNP missense variant P/S 230 151 0.15 10 benign 0.009 13001 likely benign 13
1635 ERBB2 rs759753872 SNP missense variant P/T 232 151 0.15 367 benign 0.366 14001 likely benign 14
1636 ERBB2 rs1220372519 SNP missense variant C/Y 235 31 0.03 1001 probably damaging 1 29001 likely benign 29
1637 ERBB2 rs1276981083 SNP missense variant H/R 237 1 0 987 probably damaging 0.986 26001 likely benign 26
1638 ERBB2 rs752656997 SNP missense variant A/T 241 1 0 997 probably damaging 0.996 28001 likely benign 28
1639 ERBB2 rs533090552 SNP missense variant G/S 243 1 0 1001 probably damaging 1 29001 likely benign 29
1640 ERBB2 rs767309845 SNP missense variant G/V 243 11 0.01 1001 probably damaging 1 27001 likely benign 27
1641 ERBB2 rs1443426897 SNP missense variant C/Y 244 1 0 1001 probably damaging 1 28001 likely benign 28
1642 ERBB2 rs376183465 SNP missense variant T/M 245 1 0 999 probably damaging 0.998 25001 likely benign 25
1643 ERBB2 rs779750598 SNP missense variant S/P 250 1 0 967 probably damaging 0.966 27001 likely benign 27
1644 ERBB2 rs777081311 SNP missense variant L/P 256 101 0.1 836 possibly damaging 0.835 26001 likely benign 26
1645 ERBB2 rs1567900439 SNP missense variant H/Y 257 11 0.01 593 possibly damaging 0.592 24001 likely benign 24
1646 ERBB2 rs769870618 SNP missense variant N/S 259 11 0.01 670 possibly damaging 0.669 25001 likely benign 25
1647 ERBB2 rs762919589 SNP missense variant H/Y 260 1 0 938 probably damaging 0.937 24001 likely benign 24
1648 ERBB2 rs548076348 SNP missense variant G/D 262 21 0.02 992 probably damaging 0.991 27001 likely benign 27
1649 ERBB2 rs750324803 SNP missense variant I/V 263 761 0.76 1 benign 0 17001 likely benign 17
1650 ERBB2 rs750324803 SNP missense variant I/F 263 51 0.05 366 benign 0.365 23001 likely benign 23
1651 ERBB2 rs773759626 SNP missense variant H/Y 267 41 0.04 827 possibly damaging 0.826 25001 likely benign 25
1652 ERBB2 rs200382130 SNP missense variant A/S 270 151 0.15 8 benign 0.007 14001 likely benign 14
1653 ERBB2 rs754656388 SNP missense variant A/V 270 31 0.03 28 benign 0.027 23001 likely benign 23
1654 ERBB2 rs752295912 SNP missense variant T/I 273 981 0.98 2 benign 0.001 12001 likely benign 12
1655 ERBB2 rs757811990 SNP missense variant T/K 278 1 0 975 probably damaging 0.974 25001 likely benign 25
1656 ERBB2 rs757811990 SNP missense variant T/M 278 31 0.03 899 possibly damaging 0.898 25001 likely benign 25
1657 ERBB2 rs1429013623 SNP missense variant S/Y 281 121 0.12 970 probably damaging 0.969 23001 likely benign 23
1658 ERBB2 rs778408285 SNP missense variant M/L 282 361 0.36 1 benign 0 15001 likely benign 15
1659 ERBB2 rs1161929692 SNP missense variant M/I 282 231 0.23 2 benign 0.001 20001 likely benign 20
1660 ERBB2 rs149210045 SNP missense variant E/K 286 271 0.27 168 benign 0.167 22001 likely benign 22
1661 ERBB2 rs149210045 SNP missense variant E/Q 286 251 0.25 53 benign 0.052 22001 likely benign 22
1662 ERBB2 rs1387549970 SNP missense variant R/W 288 1 0 1000 probably damaging 0.999 31001 likely deleterious 31
1663 ERBB2 rs760205387 SNP missense variant R/Q 288 1 0 962 probably damaging 0.961 29001 likely benign 29
1664 ERBB2 rs746190897 SNP missense variant T/A 290 71 0.07 46 benign 0.045 23001 likely benign 23
1665 ERBB2 rs775544453 SNP missense variant G/S 292 1 0 1001 probably damaging 1 29001 likely benign 29
1666 ERBB2 rs1258412021 SNP missense variant A/T 293 1 0 963 probably damaging 0.962 27001 likely benign 27
1667 ERBB2 rs866985163 SNP missense variant S/N 294 111 0.11 512 possibly damaging 0.511 23001 likely benign 23
1668 ERBB2 rs1191408638 SNP missense variant P/R 300 1 0 1001 probably damaging 1 31001 likely deleterious 31
1669 ERBB2 rs1191408638 SNP missense variant P/L 300 1 0 1001 probably damaging 1 32001 likely deleterious 32
1670 ERBB2 rs768855063 SNP missense variant N/S 302 1 0 1001 probably damaging 1 26001 likely benign 26
1671 ERBB2 rs768855063 SNP missense variant N/I 302 1 0 1001 probably damaging 1 25001 likely benign 25
1672 ERBB2 rs1308928763 SNP missense variant T/M 306 171 0.17 924 probably damaging 0.923 23001 likely benign 23
1673 ERBB2 rs776515406 SNP missense variant V/M 308 221 0.22 965 probably damaging 0.964 23001 likely benign 23
1674 ERBB2 rs1057519787 SNP missense variant G/E 309 1 0 1001 probably damaging 1 24001 likely benign 24
1675 ERBB2 rs1057519787 SNP missense variant G/A 309 21 0.02 998 probably damaging 0.997 24001 likely benign 24
1676 ERBB2 rs1057519816 SNP missense variant S/Y 310 1 0 996 probably damaging 0.995 24001 likely benign 24
1677 ERBB2 rs1057519816 SNP missense variant S/F 310 1 0 996 probably damaging 0.995 24001 likely benign 24
1678 ERBB2 rs775294491 SNP missense variant V/I 314 71 0.07 140 benign 0.139 18001 likely benign 18
1679 ERBB2 rs762547363 SNP missense variant H/Y 318 11 0.01 144 benign 0.143 21001 likely benign 21
1680 ERBB2 rs1396809633 SNP missense variant H/R 318 61 0.06 2 benign 0.001 21001 likely benign 21
1681 ERBB2 rs1230152304 SNP missense variant H/Q 318 31 0.03 51 benign 0.05 23001 likely benign 23
1682 ERBB2 rs1273270181 SNP missense variant Q/E 320 241 0.24 324 benign 0.323 20001 likely benign 20
1683 ERBB2 rs1301941452 SNP missense variant V/A 322 1 0 982 probably damaging 0.981 27001 likely benign 27
1684 ERBB2 rs1468532659 SNP missense variant T/S 323 561 0.56 74 benign 0.073 18001 likely benign 18
1685 ERBB2 rs1202895125 SNP missense variant E/K 325 91 0.09 113 benign 0.112 21001 likely benign 21
1686 ERBB2 rs763793826 SNP missense variant T/K 328 71 0.07 27 benign 0.026 20001 likely benign 20
1687 ERBB2 rs763793826 SNP missense variant T/I 328 841 0.84 19 benign 0.018 16001 likely benign 16
1688 ERBB2 rs761376658 SNP missense variant R/W 330 1 0 885 possibly damaging 0.884 26001 likely benign 26
1689 ERBB2 rs768206712 SNP missense variant R/Q 330 81 0.08 13 benign 0.012 23001 likely benign 23
1690 ERBB2 rs564382616 SNP missense variant C/Y 331 1 0 1001 probably damaging 1 32001 likely deleterious 32
1691 ERBB2 rs756588194 SNP missense variant E/D 332 161 0.16 25 benign 0.024 19001 likely benign 19
1692 ERBB2 rs1409114304 SNP missense variant C/Y 334 1 0 1001 probably damaging 1 27001 likely benign 27
1693 ERBB2 rs1409114304 SNP missense variant C/F 334 1 0 1001 probably damaging 1 27001 likely benign 27
1694 ERBB2 rs532077147 SNP missense variant R/Q 340 21 0.02 4 benign 0.003 22001 likely benign 22
1695 ERBB2 rs747993530 SNP missense variant Y/C 343 31 0.03 975 probably damaging 0.974 29001 likely benign 29
1696 ERBB2 rs758204762 SNP missense variant G/S 344 31 0.03 984 probably damaging 0.983 29001 likely benign 29
1697 ERBB2 rs758204762 SNP missense variant G/R 344 1 0 1000 probably damaging 0.999 28001 likely benign 28
1698 ERBB2 rs1037129509 SNP missense variant G/D 344 11 0.01 1000 probably damaging 0.999 28001 likely benign 28
1699 ERBB2 rs1460443371 SNP missense variant G/S 346 11 0.01 755 possibly damaging 0.754 28001 likely benign 28
1700 ERBB2 rs746686273 SNP missense variant M/K 347 81 0.08 16 benign 0.015 22001 likely benign 22
1701 ERBB2 rs1263270004 SNP missense variant E/G 348 1001 1 1 benign 0 23001 likely benign 23
1702 ERBB2 rs559242250 SNP missense variant L/F 350 191 0.19 405 benign 0.404 17001 likely benign 17
1703 ERBB2 rs775972596 SNP missense variant R/Q 351 651 0.65 6 benign 0.005 22001 likely benign 22
1704 ERBB2 rs763367024 SNP missense variant E/G 352 971 0.97 1 benign 0 21001 likely benign 21
1705 ERBB2 rs769082334 SNP missense variant V/M 353 81 0.08 351 benign 0.35 19001 likely benign 19
1706 ERBB2 rs769082334 SNP missense variant V/L 353 121 0.12 10 benign 0.009 17001 likely benign 17
1707 ERBB2 rs1197249604 SNP missense variant V/A 353 861 0.86 4 benign 0.003 1001 likely benign 1
1708 ERBB2 rs918747921 SNP missense variant R/W 354 21 0.02 644 possibly damaging 0.643 25001 likely benign 25
1709 ERBB2 rs1385831939 SNP missense variant T/A 357 1 0 51 benign 0.05 23001 likely benign 23
1710 ERBB2 rs373474372 SNP missense variant N/I 360 21 0.02 897 possibly damaging 0.896 27001 likely benign 27
1711 ERBB2 rs1324411001 SNP missense variant A/S 365 661 0.66 6 benign 0.005 13001 likely benign 13
1712 ERBB2 rs767588058 SNP missense variant G/R 366 11 0.01 888 possibly damaging 0.887 28001 likely benign 28
1713 ERBB2 rs1435728387 SNP missense variant G/A 366 11 0.01 563 possibly damaging 0.562 25001 likely benign 25
1714 ERBB2 rs1275492389 SNP missense variant I/M 370 1 0 1000 probably damaging 0.999 24001 likely benign 24
1715 ERBB2 rs1243660575 SNP missense variant F/C 371 171 0.17 989 probably damaging 0.988 25001 likely benign 25
1716 ERBB2 rs149567593 SNP missense variant F/L 371 601 0.6 565 possibly damaging 0.564 20001 likely benign 20
1717 ERBB2 rs752664566 SNP missense variant A/T 375 381 0.38 555 possibly damaging 0.554 24001 likely benign 24
1718 ERBB2 rs752664566 SNP missense variant A/S 375 521 0.52 407 benign 0.406 22001 likely benign 22
1719 ERBB2 rs758210687 SNP missense variant P/L 378 171 0.17 841 possibly damaging 0.84 22001 likely benign 22
1720 ERBB2 rs148068883 SNP missense variant S/G 380 501 0.5 822 possibly damaging 0.821 24001 likely benign 24
1721 ERBB2 rs1481595696 SNP missense variant D/H 382 271 0.27 4 benign 0.003 19001 likely benign 19
1722 ERBB2 rs751270411 SNP missense variant G/E 383 1 0 999 probably damaging 0.998 35001 likely deleterious 35
1723 ERBB2 rs753902259 SNP missense variant D/N 384 51 0.05 237 benign 0.236 23001 likely benign 23
1724 ERBB2 rs141116145 SNP missense variant A/D 386 141 0.14 2 benign 0.001 14001 likely benign 14
1725 ERBB2 rs141116145 SNP missense variant A/G 386 151 0.15 16 benign 0.015 14001 likely benign 14
1726 ERBB2 rs780881510 SNP missense variant N/H 388 91 0.09 54 benign 0.053 17001 likely benign 17
1727 ERBB2 rs750090147 SNP missense variant N/S 388 141 0.14 8 benign 0.007 4001 likely benign 4
1728 ERBB2 rs755701444 SNP missense variant A/T 390 101 0.1 84 benign 0.083 11001 likely benign 11
1729 ERBB2 rs587778264 SNP missense variant A/V 390 31 0.03 19 benign 0.018 11001 likely benign 11
1730 ERBB2 rs748700504 SNP missense variant P/L 391 11 0.01 732 possibly damaging 0.731 22001 likely benign 22
1731 ERBB2 rs772548631 SNP missense variant P/L 394 61 0.06 218 benign 0.217 16001 likely benign 16
1732 ERBB2 rs919231881 SNP missense variant E/Q 395 231 0.23 12 benign 0.011 15001 likely benign 15
1733 ERBB2 rs773649491 SNP missense variant Q/R 398 391 0.39 1 benign 0 1 likely benign 0
1734 ERBB2 rs747239268 SNP missense variant V/M 399 21 0.02 958 probably damaging 0.957 23001 likely benign 23
1735 ERBB2 rs377649991 SNP missense variant L/M 403 21 0.02 991 probably damaging 0.99 23001 likely benign 23
1736 ERBB2 rs1206146902 SNP missense variant I/T 406 1 0 997 probably damaging 0.996 26001 likely benign 26
1737 ERBB2 rs587778265 SNP missense variant Y/D 411 121 0.12 968 probably damaging 0.967 25001 likely benign 25
1738 ERBB2 rs758908894 SNP missense variant I/V 412 21 0.02 967 probably damaging 0.966 25001 likely benign 25
1739 ERBB2 rs747327229 SNP missense variant P/L 416 1 0 1000 probably damaging 0.999 26001 likely benign 26
1740 ERBB2 rs1337551062 SNP missense variant D/H 417 1 0 619 possibly damaging 0.618 26001 likely benign 26
1741 ERBB2 rs776714622 SNP missense variant D/A 417 111 0.11 1 benign 0 23001 likely benign 23
1742 ERBB2 rs746020984 SNP missense variant L/R 419 311 0.31 55 benign 0.054 21001 likely benign 21
1743 ERBB2 rs769778398 SNP missense variant L/I 422 1 0 994 probably damaging 0.993 24001 likely benign 24
1744 ERBB2 rs769778398 SNP missense variant L/F 422 111 0.11 1000 probably damaging 0.999 23001 likely benign 23
1745 ERBB2 rs199668084 SNP missense variant S/G 423 231 0.23 70 benign 0.069 15001 likely benign 15
1746 ERBB2 rs142783371 SNP missense variant V/I 424 101 0.1 59 benign 0.058 17001 likely benign 17
1747 ERBB2 rs891454367 SNP missense variant L/V 428 21 0.02 1001 probably damaging 1 24001 likely benign 24
1748 ERBB2 rs1322685342 SNP missense variant Q/H 429 161 0.16 4 benign 0.003 17001 likely benign 17
1749 ERBB2 rs767398280 SNP missense variant V/I 430 901 0.9 18 benign 0.017 15001 likely benign 15
1750 ERBB2 rs367606199 SNP missense variant R/W 432 1 0 1001 probably damaging 1 29001 likely benign 29
1751 ERBB2 rs1029745309 SNP missense variant R/Q 432 61 0.06 949 probably damaging 0.948 26001 likely benign 26
1752 ERBB2 rs1477349434 SNP missense variant G/R 433 21 0.02 1001 probably damaging 1 28001 likely benign 28
1753 ERBB2 rs147382623 SNP missense variant R/Q 434 1 0 954 probably damaging 0.953 29001 likely benign 29
1754 ERBB2 rs766083302 SNP missense variant H/Y 437 1001 1 6 benign 0.005 14001 likely benign 14
1755 ERBB2 rs756345214 SNP missense variant A/T 440 511 0.51 28 benign 0.027 21001 likely benign 21
1756 ERBB2 rs749440298 SNP missense variant S/L 442 481 0.48 978 probably damaging 0.977 22001 likely benign 22
1757 ERBB2 rs1351684417 SNP missense variant T/I 444 901 0.9 212 benign 0.211 16001 likely benign 16
1758 ERBB2 rs1359828514 SNP missense variant Q/E 446 771 0.77 8 benign 0.007 15001 likely benign 15
1759 ERBB2 rs930754368 SNP missense variant G/E 447 361 0.36 236 benign 0.235 21001 likely benign 21
1760 ERBB2 rs930754368 SNP missense variant G/A 447 321 0.32 84 benign 0.083 20001 likely benign 20
1761 ERBB2 rs1158382665 SNP missense variant G/S 449 531 0.53 11 benign 0.01 15001 likely benign 15
1762 ERBB2 rs770857517 SNP missense variant I/V 450 91 0.09 118 benign 0.117 19001 likely benign 19
1763 ERBB2 rs1047793418 SNP missense variant S/N 451 311 0.31 34 benign 0.033 14001 likely benign 14
1764 ERBB2 rs4252633 SNP missense variant W/C 452 111 0.11 884 possibly damaging 0.883 23001 likely benign 23
1765 ERBB2 rs759352819 SNP missense variant L/V 453 1 0 1001 probably damaging 1 24001 likely benign 24
1766 ERBB2 rs1410783126 SNP missense variant G/E 454 11 0.01 1001 probably damaging 1 26001 likely benign 26
1767 ERBB2 rs200497646 SNP missense variant R/C 456 1 0 1001 probably damaging 1 27001 likely benign 27
1768 ERBB2 rs1190280142 SNP missense variant E/D 460 11 0.01 979 probably damaging 0.978 19001 likely benign 19
1769 ERBB2 rs1457127715 SNP missense variant G/S 462 1001 1 4 benign 0.003 14001 likely benign 14
1770 ERBB2 rs1457127715 SNP missense variant G/R 462 1 0 532 possibly damaging 0.531 23001 likely benign 23
1771 ERBB2 rs373192991 SNP missense variant G/D 462 21 0.02 11 benign 0.01 23001 likely benign 23
1772 ERBB2 rs373192991 SNP missense variant G/V 462 1 0 449 possibly damaging 0.448 25001 likely benign 25
1773 ERBB2 rs1399148945 SNP missense variant G/V 464 1 0 1001 probably damaging 1 26001 likely benign 26
1774 ERBB2 rs751074421 SNP missense variant A/V 466 1001 1 1 benign 0 9001 likely benign 9
1775 ERBB2 rs1328775165 SNP missense variant L/F 467 121 0.12 629 possibly damaging 0.628 22001 likely benign 22
1776 ERBB2 rs1374683189 SNP missense variant I/T 468 1 0 876 possibly damaging 0.875 24001 likely benign 24
1777 ERBB2 rs201097345 SNP missense variant H/R 470 561 0.56 1 benign 0 1001 likely benign 1
1778 ERBB2 rs768049972 SNP missense variant T/I 472 161 0.16 42 benign 0.041 6001 likely benign 6
1779 ERBB2 rs756500045 SNP missense variant H/D 473 211 0.21 4 benign 0.003 9001 likely benign 9
1780 ERBB2 rs756500045 SNP missense variant H/Y 473 11 0.01 276 benign 0.275 14001 likely benign 14
1781 ERBB2 rs1033535912 SNP missense variant L/I 474 1 0 1001 probably damaging 1 23001 likely benign 23
1782 ERBB2 rs1033535912 SNP missense variant L/V 474 1 0 1001 probably damaging 1 23001 likely benign 23
1783 ERBB2 rs780201941 SNP missense variant F/V 476 11 0.01 986 probably damaging 0.985 26001 likely benign 26
1784 ERBB2 rs1025899392 SNP missense variant F/S 476 1 0 1000 probably damaging 0.999 27001 likely benign 27
1785 ERBB2 rs755121772 SNP missense variant V/M 477 201 0.2 235 benign 0.234 16001 likely benign 16
1786 ERBB2 rs755121772 SNP missense variant V/L 477 671 0.67 4 benign 0.003 14001 likely benign 14
1787 ERBB2 rs201021373 SNP missense variant T/M 479 21 0.02 926 probably damaging 0.925 24001 likely benign 24
1788 ERBB2 rs370565888 SNP missense variant P/L 481 431 0.43 945 probably damaging 0.944 23001 likely benign 23
1789 ERBB2 rs571837012 SNP missense variant D/N 483 471 0.47 2 benign 0.001 18001 likely benign 18
1790 ERBB2 rs1160406748 SNP missense variant D/G 483 381 0.38 6 benign 0.005 18001 likely benign 18
1791 ERBB2 rs1375073443 SNP missense variant D/E 483 991 0.99 1 benign 0 6001 likely benign 6
1792 ERBB2 rs375382055 SNP missense variant R/W 487 41 0.04 682 possibly damaging 0.681 25001 likely benign 25
1793 ERBB2 rs371450390 SNP missense variant R/Q 487 211 0.21 11 benign 0.01 22001 likely benign 22
1794 ERBB2 rs371450390 SNP missense variant R/P 487 61 0.06 526 possibly damaging 0.525 24001 likely benign 24
1795 ERBB2 rs768374532 SNP missense variant N/K 488 91 0.09 182 benign 0.181 17001 likely benign 17
1796 ERBB2 rs987507136 SNP missense variant P/S 489 571 0.57 22 benign 0.021 17001 likely benign 17
1797 ERBB2 rs142456637 SNP missense variant P/L 489 31 0.03 541 possibly damaging 0.54 24001 likely benign 24
1798 ERBB2 rs140670446 SNP missense variant Q/E 491 11 0.01 970 probably damaging 0.969 24001 likely benign 24
1799 ERBB2 rs1191789317 SNP missense variant L/V 493 781 0.78 10 benign 0.009 15001 likely benign 15
1800 ERBB2 rs879357054 SNP missense variant H/P 495 191 0.19 104 benign 0.103 20001 likely benign 20
1801 ERBB2 rs767978749 SNP missense variant T/I 496 251 0.25 2 benign 0.001 15001 likely benign 15
1802 ERBB2 rs145762641 SNP missense variant A/T 497 331 0.33 10 benign 0.009 21001 likely benign 21
1803 ERBB2 rs1277370521 SNP missense variant N/S 498 1 0 963 probably damaging 0.962 25001 likely benign 25
1804 ERBB2 rs199530208 SNP missense variant R/G 499 21 0.02 233 benign 0.232 23001 likely benign 23
1805 ERBB2 rs199530208 SNP missense variant R/W 499 1 0 846 possibly damaging 0.845 27001 likely benign 27
1806 ERBB2 rs182572604 SNP missense variant R/Q 499 281 0.28 7 benign 0.006 21001 likely benign 21
1807 ERBB2 rs182572604 SNP missense variant R/L 499 61 0.06 11 benign 0.01 22001 likely benign 22
1808 ERBB2 rs920792523 SNP missense variant P/S 500 521 0.52 1 benign 0 19001 likely benign 19
1809 ERBB2 rs1482645941 SNP missense variant E/K 501 351 0.35 4 benign 0.003 22001 likely benign 22
1810 ERBB2 rs1482645941 SNP missense variant E/Q 501 341 0.34 2 benign 0.001 21001 likely benign 21
1811 ERBB2 rs1198314054 SNP missense variant D/Y 502 11 0.01 58 benign 0.057 14001 likely benign 14
1812 ERBB2 rs752759368 SNP missense variant D/E 502 1001 1 1 benign 0 1 likely benign 0
1813 ERBB2 rs758497995 SNP missense variant E/K 503 551 0.55 20 benign 0.019 22001 likely benign 22
1814 ERBB2 rs983576212 SNP missense variant E/D 503 441 0.44 1 benign 0 15001 likely benign 15
1815 ERBB2 rs1358325733 SNP missense variant G/S 506 501 0.5 1 benign 0 10001 likely benign 10
1816 ERBB2 rs1293998208 SNP missense variant E/K 507 201 0.2 1 benign 0 9001 likely benign 9
1817 ERBB2 rs1377085949 SNP missense variant H/Y 512 581 0.58 1 benign 0 1 likely benign 0
1818 ERBB2 rs1238891256 SNP missense variant Q/H 513 311 0.31 1 benign 0 1 likely benign 0
1819 ERBB2 rs371623072 SNP missense variant A/T 516 261 0.26 10 benign 0.009 17001 likely benign 17
1820 ERBB2 rs759579850 SNP missense variant R/Q 517 481 0.48 1 benign 0 14001 likely benign 14
1821 ERBB2 rs759579850 SNP missense variant R/P 517 261 0.26 1 benign 0 16001 likely benign 16
1822 ERBB2 rs561322621 SNP missense variant G/D 522 1 0 1001 probably damaging 1 28001 likely benign 28
1823 ERBB2 rs561322621 SNP missense variant G/V 522 11 0.01 1001 probably damaging 1 27001 likely benign 27
1824 ERBB2 rs202202058 SNP missense variant P/S 523 51 0.05 801 possibly damaging 0.8 25001 likely benign 25
1825 ERBB2 rs1176949914 SNP missense variant G/E 524 91 0.09 893 possibly damaging 0.892 24001 likely benign 24
1826 ERBB2 rs1317541157 SNP missense variant Q/H 527 91 0.09 83 benign 0.082 22001 likely benign 22
1827 ERBB2 rs747838206 SNP missense variant V/I 529 71 0.07 7 benign 0.006 20001 likely benign 20
1828 ERBB2 rs771580372 SNP missense variant N/S 530 1001 1 1 benign 0 15001 likely benign 15
1829 ERBB2 rs140711914 SNP missense variant C/R 531 1 0 1001 probably damaging 1 29001 likely benign 29
1830 ERBB2 rs777363214 SNP missense variant S/R 532 1001 1 2 benign 0.001 13001 likely benign 13
1831 ERBB2 rs746476368 SNP missense variant L/F 535 711 0.71 584 possibly damaging 0.583 23001 likely benign 23
1832 ERBB2 rs140980495 SNP missense variant R/Q 536 1 0 998 probably damaging 0.997 32001 likely deleterious 32
1833 ERBB2 rs866163885 SNP missense variant G/S 537 41 0.04 303 benign 0.302 24001 likely benign 24
1834 ERBB2 rs866163885 SNP missense variant G/R 537 81 0.08 414 benign 0.413 23001 likely benign 23
1835 ERBB2 rs777116958 SNP missense variant Q/H 538 151 0.15 2 benign 0.001 16001 likely benign 16
1836 ERBB2 rs1415101808 SNP missense variant V/M 541 11 0.01 905 possibly damaging 0.904 27001 likely benign 27
1837 ERBB2 rs150203173 SNP missense variant R/Q 545 1 0 40 benign 0.039 24001 likely benign 24
1838 ERBB2 rs565582943 SNP missense variant Q/K 548 221 0.22 1 benign 0 19001 likely benign 19
1839 ERBB2 rs532713027 SNP missense variant G/W 549 1 0 1000 probably damaging 0.999 14001 likely benign 14
1840 ERBB2 rs1224275634 SNP missense variant L/V 550 271 0.27 2 benign 0.001 11001 likely benign 11
1841 ERBB2 rs1430713880 SNP missense variant A/V 557 1 0 8 benign 0.007 16001 likely benign 16
1842 ERBB2 rs767713671 SNP missense variant H/Q 559 341 0.34 1 benign 0 12001 likely benign 12
1843 ERBB2 rs201470725 SNP missense variant P/L 562 151 0.15 4 benign 0.003 16001 likely benign 16
1844 ERBB2 rs1299172694 SNP missense variant P/R 565 1 0 373 benign 0.372 22001 likely benign 22
1845 ERBB2 rs1398622638 SNP missense variant C/R 567 1 0 1000 probably damaging 0.999 27001 likely benign 27
1846 ERBB2 rs1285769371 SNP missense variant Q/E 568 251 0.25 6 benign 0.005 17001 likely benign 17
1847 ERBB2 rs763863372 SNP missense variant P/L 569 141 0.14 63 benign 0.062 22001 likely benign 22
1848 ERBB2 rs1218756471 SNP missense variant Q/E 570 481 0.48 821 possibly damaging 0.82 22001 likely benign 22
1849 ERBB2 rs756836001 SNP missense variant G/V 572 21 0.02 277 benign 0.276 22001 likely benign 22
1850 ERBB2 rs1195763693 SNP missense variant V/M 574 121 0.12 74 benign 0.073 19001 likely benign 19
1851 ERBB2 rs778479390 SNP missense variant F/C 577 181 0.18 269 benign 0.268 13001 likely benign 13
1852 ERBB2 rs1252848592 SNP missense variant G/E 578 1 0 999 probably damaging 0.998 25001 likely benign 25
1853 ERBB2 rs756686824 SNP missense variant P/L 579 41 0.04 8 benign 0.007 23001 likely benign 23
1854 ERBB2 rs1287673125 SNP missense variant V/E 585 161 0.16 1 benign 0 19001 likely benign 19
1855 ERBB2 rs1237088846 SNP missense variant H/Y 589 1 0 967 probably damaging 0.966 24001 likely benign 24
1856 ERBB2 rs767216520 SNP missense variant K/M 591 61 0.06 67 benign 0.066 22001 likely benign 22
1857 ERBB2 rs931758036 SNP missense variant D/E 592 1 0 1000 probably damaging 0.999 19001 likely benign 19
1858 ERBB2 rs750092447 SNP missense variant P/L 593 1 0 29 benign 0.028 18001 likely benign 18
1859 ERBB2 rs760310908 SNP missense variant P/H 594 11 0.01 560 possibly damaging 0.559 22001 likely benign 22
1860 ERBB2 rs755483857 SNP missense variant V/M 597 1 0 997 probably damaging 0.996 27001 likely benign 27
1861 ERBB2 rs145409713 SNP missense variant A/D 598 231 0.23 6 benign 0.005 19001 likely benign 19
1862 ERBB2 rs145409713 SNP missense variant A/G 598 91 0.09 47 benign 0.046 19001 likely benign 19
1863 ERBB2 rs369903296 SNP missense variant R/C 599 1 0 891 possibly damaging 0.89 25001 likely benign 25
1864 ERBB2 rs758820578 SNP missense variant R/H 599 261 0.26 11 benign 0.01 18001 likely benign 18
1865 ERBB2 rs747200104 SNP missense variant S/R 602 121 0.12 677 possibly damaging 0.676 14001 likely benign 14
1866 ERBB2 rs771145294 SNP missense variant G/S 603 11 0.01 999 probably damaging 0.998 28001 likely benign 28
1867 ERBB2 rs781179380 SNP missense variant G/D 603 1 0 999 probably damaging 0.998 27001 likely benign 27
1868 ERBB2 rs1282253805 SNP missense variant K/T 605 151 0.15 598 possibly damaging 0.597 24001 likely benign 24
1869 ERBB2 rs1282253805 SNP missense variant K/R 605 451 0.45 328 benign 0.327 22001 likely benign 22
1870 ERBB2 rs1219238007 SNP missense variant D/N 607 131 0.13 36 benign 0.035 23001 likely benign 23
1871 ERBB2 rs1256869007 SNP missense variant D/G 607 241 0.24 386 benign 0.385 23001 likely benign 23
1872 ERBB2 rs1304926892 SNP missense variant S/F 609 1 0 37 benign 0.036 23001 likely benign 23
1873 ERBB2 rs774261411 SNP missense variant Y/H 610 561 0.56 128 benign 0.127 22001 likely benign 22
1874 ERBB2 rs377370642 SNP missense variant M/V 611 441 0.44 1 benign 0 19001 likely benign 19
1875 ERBB2 rs1312573525 SNP missense variant K/R 615 1 0 991 probably damaging 0.99 28001 likely benign 28
1876 ERBB2 rs1413869243 SNP missense variant F/L 616 1 0 29 benign 0.028 21001 likely benign 21
1877 ERBB2 rs766029214 SNP missense variant A/T 622 471 0.47 1 benign 0 12001 likely benign 12
1878 ERBB2 rs759078493 SNP missense variant P/L 625 311 0.31 2 benign 0.001 14001 likely benign 14
1879 ERBB2 rs1173337736 SNP missense variant P/S 627 111 0.11 109 benign 0.108 22001 likely benign 22
1880 ERBB2 rs1412157429 SNP missense variant I/L 628 321 0.32 8 benign 0.007 22001 likely benign 22
1881 ERBB2 rs753267835 SNP missense variant N/D 629 1 0 923 probably damaging 0.922 27001 likely benign 27
1882 ERBB2 rs758907167 SNP missense variant N/T 629 21 0.02 666 possibly damaging 0.665 26001 likely benign 26
1883 ERBB2 rs1258745095 SNP missense variant T/S 631 101 0.1 186 benign 0.185 21001 likely benign 21
1884 ERBB2 rs778312796 SNP missense variant H/Y 632 1001 1 12 benign 0.011 18001 likely benign 18
1885 ERBB2 rs199726056 SNP missense variant S/F 633 1 0 556 possibly damaging 0.555 25001 likely benign 25
1886 ERBB2 rs367599823 SNP missense variant P/R 643 61 0.06 249 benign 0.248 23001 likely benign 23
1887 ERBB2 rs750665964 SNP missense variant A/T 644 431 0.43 12 benign 0.011 22001 likely benign 22
1888 ERBB2 rs370514427 SNP missense variant E/K 645 761 0.76 12 benign 0.011 23001 likely benign 23
1889 ERBB2 rs201784472 SNP missense variant R/K 647 851 0.85 1 benign 0 22001 likely benign 22
1890 ERBB2 rs201784472 SNP missense variant R/T 647 391 0.39 46 benign 0.045 22001 likely benign 22
1891 ERBB2 rs777759226 SNP missense variant A/T 648 741 0.74 13 benign 0.012 20001 likely benign 20
1892 ERBB2 rs1332779143 SNP missense variant P/S 650 181 0.18 4 benign 0.003 22001 likely benign 22
1893 ERBB2 rs778798172 SNP missense variant P/L 650 111 0.11 1 benign 0 22001 likely benign 22
1894 ERBB2 rs1801201 SNP missense variant I/L 654 221 0.22 86 benign 0.085 22001 likely benign 22
1895 ERBB2 rs1801201 SNP missense variant I/V 654 171 0.17 86 benign 0.085 22001 likely benign 22
1896 ERBB2 rs1136201 SNP missense variant I/V 655 751 0.75 109 benign 0.108 19001 likely benign 19
1897 ERBB2 rs1136201 SNP missense variant I/F 655 41 0.04 734 possibly damaging 0.733 26001 likely benign 26
1898 ERBB2 rs1317387900 SNP missense variant G/S 660 61 0.06 865 possibly damaging 0.864 27001 likely benign 27
1899 ERBB2 rs1196929947 SNP missense variant G/D 660 1 0 992 probably damaging 0.991 27001 likely benign 27
1900 ERBB2 rs762407538 SNP missense variant I/V 661 941 0.94 1 benign 0 1 likely benign 0
1901 ERBB2 rs1483724551 SNP missense variant L/V 662 181 0.18 409 benign 0.408 18001 likely benign 18
1902 ERBB2 rs1567911318 SNP missense variant V/M 665 61 0.06 43 benign 0.042 2001 likely benign 2
1903 ERBB2 rs372616729 SNP missense variant G/R 668 101 0.1 106 benign 0.105 15001 likely benign 15
1904 ERBB2 rs372616729 SNP missense variant G/R 668 101 0.1 106 benign 0.105 15001 likely benign 15
1905 ERBB2 rs900792840 SNP missense variant V/M 669 31 0.03 58 benign 0.057 6001 likely benign 6
1906 ERBB2 rs1312937127 SNP missense variant V/G 670 481 0.48 105 benign 0.104 15001 likely benign 15
1907 ERBB2 rs1168496712 SNP missense variant F/L 671 1001 1 1 benign 0 1 likely benign 0
1908 ERBB2 rs1423654581 SNP missense variant I/N 673 1 0 43 benign 0.042 20001 likely benign 20
1909 ERBB2 rs996814735 SNP missense variant I/V 675 771 0.77 7 benign 0.006 4001 likely benign 4
1910 ERBB2 rs1418604945 SNP missense variant K/M 676 131 0.13 8 benign 0.007 22001 likely benign 22
1911 ERBB2 rs1167835335 SNP missense variant R/Q 677 1 0 1000 probably damaging 0.999 29001 likely benign 29
1912 ERBB2 rs1377979176 SNP missense variant R/W 678 1 0 119 benign 0.118 17001 likely benign 17
1913 ERBB2 rs1057519862 SNP missense variant R/Q 678 191 0.19 104 benign 0.103 23001 likely benign 23
1914 ERBB2 rs759608479 SNP missense variant Q/E 679 21 0.02 1 benign 0 19001 likely benign 19
1915 ERBB2 rs765387989 SNP missense variant R/Q 683 1 0 939 probably damaging 0.938 31001 likely deleterious 31
1916 ERBB2 rs765387989 SNP missense variant R/P 683 1 0 986 probably damaging 0.985 32001 likely deleterious 32
1917 ERBB2 rs1302627802 SNP missense variant K/R 684 81 0.08 832 possibly damaging 0.831 26001 likely benign 26
1918 ERBB2 rs752669313 SNP missense variant Y/H 685 161 0.16 1 benign 0 23001 likely benign 23
1919 ERBB2 rs1190122730 SNP missense variant T/M 686 1 0 997 probably damaging 0.996 26001 likely benign 26
1920 ERBB2 rs1402335179 SNP missense variant M/L 687 1001 1 20 benign 0.019 19001 likely benign 19
1921 ERBB2 rs867851148 SNP missense variant Q/K 692 61 0.06 984 probably damaging 0.983 24001 likely benign 24
1922 ERBB2 rs1192572638 SNP missense variant P/T 699 1 0 1001 probably damaging 1 26001 likely benign 26
1923 ERBB2 rs1441217225 SNP missense variant T/I 701 1 0 993 probably damaging 0.992 27001 likely benign 27
1924 ERBB2 rs34602395 SNP missense variant S/I 703 1 0 1001 probably damaging 1 27001 likely benign 27
1925 ERBB2 rs868026167 SNP missense variant G/R 704 1 0 1001 probably damaging 1 31001 likely deleterious 31
1926 ERBB2 rs1265427684 SNP missense variant N/K 708 1 0 990 probably damaging 0.989 24001 likely benign 24
1927 ERBB2 rs959346230 SNP missense variant Q/K 709 31 0.03 998 probably damaging 0.997 25001 likely benign 25
1928 ERBB2 rs991114244 SNP missense variant M/L 712 1001 1 8 benign 0.007 19001 likely benign 19
1929 ERBB2 rs756073738 SNP missense variant M/R 712 1 0 886 possibly damaging 0.885 28001 likely benign 28
1930 ERBB2 rs779034594 SNP missense variant R/Q 713 1 0 999 probably damaging 0.998 32001 likely deleterious 32
1931 ERBB2 rs967815855 SNP missense variant E/K 719 1 0 953 probably damaging 0.952 29001 likely benign 29
1932 ERBB2 rs977818812 SNP missense variant E/V 719 1 0 991 probably damaging 0.99 31001 likely deleterious 31
1933 ERBB2 rs1221984925 SNP missense variant V/M 723 41 0.04 63 benign 0.062 23001 likely benign 23
1934 ERBB2 rs1452141491 SNP missense variant A/T 730 1 0 1001 probably damaging 1 31001 likely deleterious 31
19