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 |
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 |