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 |
63841 |
PMS2 |
rs36038802 |
SNP |
missense variant |
Q/K |
160 |
101 |
0.1 |
590 |
possibly damaging |
0.589 |
|
|
|
63842 |
PMS2 |
rs142416537 |
SNP |
missense variant |
V/L |
159 |
571 |
0.57 |
60 |
benign |
0.059 |
|
|
|
63843 |
PMS2 |
rs142416537 |
SNP |
missense variant |
V/M |
159 |
1 |
0 |
961 |
probably damaging |
0.96 |
|
|
|
63844 |
PMS2 |
rs750354871 |
SNP |
missense variant |
S/I |
158 |
1 |
0 |
756 |
possibly damaging |
0.755 |
|
|
|
63845 |
PMS2 |
rs786204206 |
SNP |
missense variant |
T/A |
156 |
1 |
0 |
997 |
probably damaging |
0.996 |
|
|
|
63846 |
PMS2 |
rs779013546 |
SNP |
missense variant |
R/G |
153 |
71 |
0.07 |
36 |
benign |
0.035 |
|
|
|
63847 |
PMS2 |
rs876660161 |
SNP |
missense variant |
P/R |
152 |
191 |
0.19 |
953 |
probably damaging |
0.952 |
|
|
|
63848 |
PMS2 |
rs35629870 |
SNP |
missense variant |
R/H |
151 |
1 |
0 |
877 |
possibly damaging |
0.876 |
|
|
|
63849 |
PMS2 |
rs758561884 |
SNP |
missense variant |
R/C |
151 |
1 |
0 |
1000 |
probably damaging |
0.999 |
|
|
|
63850 |
PMS2 |
rs778119115 |
SNP |
missense variant |
P/L |
150 |
1 |
0 |
975 |
probably damaging |
0.974 |
|
|
|