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 |
61101 |
PBRM1 |
rs763433177 |
SNP |
missense variant |
Y/F |
390 |
381 |
0.38 |
988 |
probably damaging |
0.987 |
|
|
|
61102 |
PBRM1 |
rs935520845 |
SNP |
missense variant |
L/I |
389 |
1 |
0 |
327 |
benign |
0.326 |
|
|
|
61103 |
PBRM1 |
rs866423710 |
SNP |
missense variant |
Q/H |
388 |
1 |
0 |
992 |
probably damaging |
0.991 |
|
|
|
61104 |
PBRM1 |
rs764381947 |
SNP |
missense variant |
F/S |
386 |
311 |
0.31 |
23 |
benign |
0.022 |
|
|
|
61105 |
PBRM1 |
rs913417875 |
SNP |
missense variant |
N/H |
384 |
1 |
0 |
886 |
possibly damaging |
0.885 |
|
|
|
61106 |
PBRM1 |
rs751885636 |
SNP |
missense variant |
S/L |
383 |
21 |
0.02 |
273 |
benign |
0.272 |
|
|
|
61107 |
PBRM1 |
rs767987709 |
SNP |
missense variant |
D/G |
381 |
11 |
0.01 |
521 |
possibly damaging |
0.52 |
|
|
|
61108 |
PBRM1 |
rs896608828 |
SNP |
missense variant |
S/A |
378 |
11 |
0.01 |
970 |
probably damaging |
0.969 |
|
|
|
61109 |
PBRM1 |
rs373477703 |
SNP |
missense variant |
Y/C |
366 |
71 |
0.07 |
998 |
probably damaging |
0.997 |
|
|
|
61110 |
PBRM1 |
rs373477703 |
SNP |
missense variant |
Y/S |
366 |
211 |
0.21 |
995 |
probably damaging |
0.994 |
|
|
|