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 |
9471 |
KM2TC-MLL3 |
rs1381538083 |
SNP |
missense variant |
K/N |
822 |
1 |
0 |
998 |
probably damaging |
0.997 |
25001 |
likely benign |
25 |
9472 |
KM2TC-MLL3 |
rs778616260 |
SNP |
missense variant |
K/I |
822 |
1 |
0 |
999 |
probably damaging |
0.998 |
31001 |
likely deleterious |
31 |
9473 |
KM2TC-MLL3 |
rs778616260 |
SNP |
missense variant |
K/T |
822 |
1 |
0 |
998 |
probably damaging |
0.997 |
28001 |
likely benign |
28 |
9474 |
KM2TC-MLL3 |
rs1156313947 |
SNP |
missense variant |
K/E |
822 |
1 |
0 |
995 |
probably damaging |
0.994 |
29001 |
likely benign |
29 |
9475 |
KM2TC-MLL3 |
rs1383545815 |
SNP |
missense variant |
P/L |
821 |
1 |
0 |
998 |
probably damaging |
0.997 |
31001 |
likely deleterious |
31 |
9476 |
KM2TC-MLL3 |
rs748010370 |
SNP |
missense variant |
P/A |
821 |
1 |
0 |
997 |
probably damaging |
0.996 |
26001 |
likely benign |
26 |
9477 |
KM2TC-MLL3 |
rs748010370 |
SNP |
missense variant |
P/T |
821 |
1 |
0 |
998 |
probably damaging |
0.997 |
27001 |
likely benign |
27 |
9478 |
KM2TC-MLL3 |
rs200598064 |
SNP |
missense variant |
T/I |
820 |
1 |
0 |
547 |
possibly damaging |
0.546 |
27001 |
likely benign |
27 |
9479 |
KM2TC-MLL3 |
rs200598064 |
SNP |
missense variant |
T/S |
820 |
11 |
0.01 |
198 |
benign |
0.197 |
23001 |
likely benign |
23 |
9480 |
KM2TC-MLL3 |
rs1347731630 |
SNP |
missense variant |
V/G |
819 |
1 |
0 |
638 |
possibly damaging |
0.637 |
27001 |
likely benign |
27 |