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 |
25431 |
MLL2 |
rs1339906244 |
SNP |
missense variant |
C/R |
1477 |
1 |
0 |
1000 |
probably damaging |
0.999 |
28001 |
likely benign |
28 |
25432 |
MLL2 |
rs1227169455 |
SNP |
missense variant |
S/C |
1476 |
231 |
0.23 |
14 |
benign |
0.013 |
22001 |
likely benign |
22 |
25433 |
MLL2 |
rs587783718 |
SNP |
missense variant |
C/Y |
1474 |
1 |
0 |
1000 |
probably damaging |
0.999 |
26001 |
likely benign |
26 |
25434 |
MLL2 |
rs767466146 |
SNP |
missense variant |
W/C |
1473 |
1 |
0 |
1001 |
probably damaging |
1 |
|
- |
|
25435 |
MLL2 |
rs1377104637 |
SNP |
missense variant |
K/N |
1472 |
1 |
0 |
986 |
probably damaging |
0.985 |
24001 |
likely benign |
24 |
25436 |
MLL2 |
rs794727144 |
SNP |
missense variant |
K/E |
1472 |
1 |
0 |
966 |
probably damaging |
0.965 |
29001 |
likely benign |
29 |
25437 |
MLL2 |
rs773072573 |
SNP |
missense variant |
G/C |
1468 |
1 |
0 |
1001 |
probably damaging |
1 |
27001 |
likely benign |
27 |
25438 |
MLL2 |
rs1049363934 |
SNP |
missense variant |
K/R |
1466 |
11 |
0.01 |
999 |
probably damaging |
0.998 |
27001 |
likely benign |
27 |
25439 |
MLL2 |
rs1474346582 |
SNP |
missense variant |
V/I |
1464 |
1 |
0 |
998 |
probably damaging |
0.997 |
24001 |
likely benign |
24 |
25440 |
MLL2 |
rs1262943788 |
SNP |
missense variant |
P/L |
1460 |
1 |
0 |
1000 |
probably damaging |
0.999 |
28001 |
likely benign |
28 |