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 |
31851 |
MLH1 |
rs63750610 |
SNP |
missense variant |
P/R |
550 |
1 |
0 |
1001 |
probably damaging |
1 |
24001 |
likely benign |
24 |
31852 |
MLH1 |
rs63750610 |
SNP |
missense variant |
P/L |
550 |
1 |
0 |
1001 |
probably damaging |
1 |
24001 |
likely benign |
24 |
31853 |
MLH1 |
rs1280930048 |
SNP |
missense variant |
P/S |
551 |
521 |
0.52 |
29 |
benign |
0.028 |
17001 |
likely benign |
17 |
31854 |
MLH1 |
rs1553663957 |
SNP |
missense variant |
L/S |
552 |
11 |
0.01 |
697 |
possibly damaging |
0.696 |
25001 |
likely benign |
25 |
31855 |
MLH1 |
rs63751202 |
SNP |
missense variant |
L/P |
555 |
1 |
0 |
999 |
probably damaging |
0.998 |
29001 |
likely benign |
29 |
31856 |
MLH1 |
rs63751202 |
SNP |
missense variant |
L/R |
555 |
1 |
0 |
997 |
probably damaging |
0.996 |
28001 |
likely benign |
28 |
31857 |
MLH1 |
rs1559591314 |
SNP |
missense variant |
P/S |
556 |
1 |
0 |
1001 |
probably damaging |
1 |
26001 |
likely benign |
26 |
31858 |
MLH1 |
rs63750726 |
SNP |
missense variant |
P/L |
556 |
1 |
0 |
1001 |
probably damaging |
1 |
26001 |
likely benign |
26 |
31859 |
MLH1 |
rs55907433 |
SNP |
missense variant |
I/V |
557 |
31 |
0.03 |
2 |
benign |
0.001 |
16001 |
likely benign |
16 |
31860 |
MLH1 |
rs55907433 |
SNP |
missense variant |
I/F |
557 |
21 |
0.02 |
50 |
benign |
0.049 |
22001 |
likely benign |
22 |