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 |
50201 |
MEN1 |
rs1114167517 |
sequence alteration |
missense variant |
K/E |
562 |
1 |
0 |
990 |
probably damaging |
0.989 |
|
|
|
50202 |
MEN1 |
rs863224527 |
SNP |
missense variant |
S/N |
560 |
1 |
0 |
983 |
probably damaging |
0.982 |
|
|
|
50203 |
MEN1 |
rs878886267 |
SNP |
missense variant |
T/I |
557 |
241 |
0.24 |
18 |
benign |
0.017 |
|
|
|
50204 |
MEN1 |
rs121913035 |
SNP |
missense variant |
T/S |
557 |
281 |
0.28 |
29 |
benign |
0.028 |
|
|
|
50205 |
MEN1 |
rs990141724 |
SNP |
missense variant |
L/F |
556 |
11 |
0.01 |
605 |
possibly damaging |
0.604 |
|
|
|
50206 |
MEN1 |
rs562257963 |
SNP |
missense variant |
V/L |
555 |
491 |
0.49 |
118 |
benign |
0.117 |
|
|
|
50207 |
MEN1 |
rs562257963 |
SNP |
missense variant |
V/L |
555 |
491 |
0.49 |
118 |
benign |
0.117 |
|
|
|
50208 |
MEN1 |
rs914488914 |
SNP |
missense variant |
E/G |
552 |
371 |
0.37 |
2 |
benign |
0.001 |
|
|
|
50209 |
MEN1 |
rs779413959 |
SNP |
missense variant |
P/L |
551 |
41 |
0.04 |
2 |
benign |
0.001 |
|
|
|
50210 |
MEN1 |
rs779413959 |
SNP |
missense variant |
P/Q |
551 |
101 |
0.1 |
19 |
benign |
0.018 |
|
|
|