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 |
32031 |
NOTCH1 |
rs1204244687 |
SNP |
missense variant |
N/S |
2528 |
461 |
0.46 |
643 |
possibly damaging |
0.642 |
23001 |
likely benign |
23 |
32032 |
NOTCH1 |
rs567323027 |
SNP |
missense variant |
P/L |
2525 |
1 |
0 |
835 |
possibly damaging |
0.834 |
28001 |
likely benign |
28 |
32033 |
NOTCH1 |
rs1554826328 |
SNP |
missense variant |
S/L |
2523 |
1 |
0 |
1000 |
probably damaging |
0.999 |
29001 |
likely benign |
29 |
32034 |
NOTCH1 |
rs1405124840 |
SNP |
missense variant |
S/N |
2522 |
1 |
0 |
999 |
probably damaging |
0.998 |
25001 |
likely benign |
25 |
32035 |
NOTCH1 |
rs771410115 |
SNP |
missense variant |
D/E |
2518 |
191 |
0.19 |
1000 |
probably damaging |
0.999 |
23001 |
likely benign |
23 |
32036 |
NOTCH1 |
rs868747222 |
SNP |
missense variant |
S/Y |
2516 |
1 |
0 |
1000 |
probably damaging |
0.999 |
28001 |
likely benign |
28 |
32037 |
NOTCH1 |
rs1365732147 |
SNP |
missense variant |
E/D |
2515 |
121 |
0.12 |
677 |
possibly damaging |
0.676 |
23001 |
likely benign |
23 |
32038 |
NOTCH1 |
rs1564567473 |
SNP |
missense variant |
P/L |
2514 |
1 |
0 |
921 |
probably damaging |
0.92 |
28001 |
likely benign |
28 |
32039 |
NOTCH1 |
rs1160184715 |
SNP |
missense variant |
P/L |
2512 |
1 |
0 |
1001 |
probably damaging |
1 |
29001 |
likely benign |
29 |
32040 |
NOTCH1 |
rs1554826340 |
SNP |
missense variant |
L/P |
2510 |
1 |
0 |
1001 |
probably damaging |
1 |
30001 |
likely deleterious |
30 |