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 |
25441 |
MLL2 |
rs1330442423 |
SNP |
missense variant |
P/S |
1460 |
1 |
0 |
1000 |
probably damaging |
0.999 |
26001 |
likely benign |
26 |
25442 |
MLL2 |
rs797045666 |
SNP |
missense variant |
C/S |
1456 |
1 |
0 |
999 |
probably damaging |
0.998 |
26001 |
likely benign |
26 |
25443 |
MLL2 |
rs767737749 |
SNP |
missense variant |
H/Q |
1453 |
1 |
0 |
1000 |
probably damaging |
0.999 |
23001 |
likely benign |
23 |
25444 |
MLL2 |
rs750735377 |
SNP |
missense variant |
I/V |
1450 |
141 |
0.14 |
307 |
benign |
0.306 |
20001 |
likely benign |
20 |
25445 |
MLL2 |
rs587783716 |
SNP |
missense variant |
C/Y |
1448 |
1 |
0 |
1000 |
probably damaging |
0.999 |
26001 |
likely benign |
26 |
25446 |
MLL2 |
rs398123746 |
SNP |
missense variant |
C/R |
1448 |
1 |
0 |
1000 |
probably damaging |
0.999 |
29001 |
likely benign |
29 |
25447 |
MLL2 |
rs398123746 |
SNP |
missense variant |
C/S |
1448 |
11 |
0.01 |
999 |
probably damaging |
0.998 |
27001 |
likely benign |
27 |
25448 |
MLL2 |
rs375891492 |
SNP |
missense variant |
R/L |
1441 |
1 |
0 |
1000 |
probably damaging |
0.999 |
27001 |
likely benign |
27 |
25449 |
MLL2 |
rs910695111 |
SNP |
missense variant |
R/C |
1441 |
1 |
0 |
1000 |
probably damaging |
0.999 |
31001 |
likely deleterious |
31 |
25450 |
MLL2 |
rs1396382997 |
SNP |
missense variant |
D/N |
1438 |
11 |
0.01 |
997 |
probably damaging |
0.996 |
27001 |
likely benign |
27 |