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 |
10431 |
ARID1B |
rs1453256339 |
SNP |
missense variant |
G/R |
319 |
11 |
0.01 |
992 |
probably damaging |
0.991 |
25001 |
likely benign |
25 |
10432 |
ARID1B |
rs1453256339 |
SNP |
missense variant |
G/R |
319 |
11 |
0.01 |
992 |
probably damaging |
0.991 |
25001 |
likely benign |
25 |
10433 |
ARID1B |
rs1193518744 |
SNP |
missense variant |
G/E |
319 |
21 |
0.02 |
989 |
probably damaging |
0.988 |
25001 |
likely benign |
25 |
10434 |
ARID1B |
rs1387109269 |
SNP |
missense variant |
G/A |
320 |
841 |
0.84 |
960 |
probably damaging |
0.959 |
22001 |
likely benign |
22 |
10435 |
ARID1B |
rs1057522183 |
SNP |
missense variant |
G/A |
321 |
1001 |
1 |
960 |
probably damaging |
0.959 |
22001 |
likely benign |
22 |
10436 |
ARID1B |
rs1399325046 |
SNP |
missense variant |
G/A |
322 |
121 |
0.12 |
960 |
probably damaging |
0.959 |
23001 |
likely benign |
23 |
10437 |
ARID1B |
rs1159915692 |
SNP |
missense variant |
G/E |
323 |
211 |
0.21 |
27 |
benign |
0.026 |
23001 |
likely benign |
23 |
10438 |
ARID1B |
rs1159915692 |
SNP |
missense variant |
G/A |
323 |
891 |
0.89 |
18 |
benign |
0.017 |
20001 |
likely benign |
20 |
10439 |
ARID1B |
rs1455234951 |
SNP |
missense variant |
G/A |
324 |
1001 |
1 |
11 |
benign |
0.01 |
19001 |
likely benign |
19 |
10440 |
ARID1B |
rs780126064 |
SNP |
missense variant |
G/R |
325 |
1 |
0 |
980 |
probably damaging |
0.979 |
24001 |
likely benign |
24 |