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 |
31331 |
MLH1 |
rs1553646744 |
SNP |
missense variant |
P/A |
192 |
31 |
0.03 |
1000 |
probably damaging |
0.999 |
25001 |
likely benign |
25 |
31332 |
MLH1 |
rs63750517 |
SNP |
missense variant |
L/P |
194 |
1 |
0 |
982 |
probably damaging |
0.981 |
31001 |
likely deleterious |
31 |
31333 |
MLH1 |
rs587779049 |
SNP |
missense variant |
Y/D |
195 |
1 |
0 |
1001 |
probably damaging |
1 |
29001 |
likely benign |
29 |
31334 |
MLH1 |
rs63751598 |
SNP |
missense variant |
S/R |
197 |
1 |
0 |
988 |
probably damaging |
0.987 |
14001 |
likely benign |
14 |
31335 |
MLH1 |
rs63751598 |
SNP |
missense variant |
S/G |
197 |
1 |
0 |
703 |
possibly damaging |
0.702 |
24001 |
likely benign |
24 |
31336 |
MLH1 |
rs63750144 |
SNP |
missense variant |
S/N |
197 |
1 |
0 |
989 |
probably damaging |
0.988 |
35001 |
likely deleterious |
35 |
31337 |
MLH1 |
rs63750144 |
SNP |
missense variant |
S/T |
197 |
1 |
0 |
953 |
probably damaging |
0.952 |
35001 |
likely deleterious |
35 |
31338 |
MLH1 |
rs63750547 |
SNP |
missense variant |
L/S |
198 |
1 |
0 |
998 |
probably damaging |
0.997 |
28001 |
likely benign |
28 |
31339 |
MLH1 |
rs63750736 |
SNP |
missense variant |
E/K |
199 |
21 |
0.02 |
286 |
benign |
0.285 |
23001 |
likely benign |
23 |
31340 |
MLH1 |
rs876658827 |
SNP |
missense variant |
S/G |
201 |
301 |
0.3 |
217 |
benign |
0.216 |
21001 |
likely benign |
21 |