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 |
20731 |
CCREBBP |
rs945398646 |
SNP |
missense variant |
V/I |
1449 |
31 |
0.03 |
963 |
probably damaging |
0.962 |
26001 |
likely benign |
26 |
20732 |
CCREBBP |
rs1470080284 |
SNP |
missense variant |
A/D |
1448 |
131 |
0.13 |
997 |
probably damaging |
0.996 |
25001 |
likely benign |
25 |
20733 |
CCREBBP |
rs1057519884 |
SNP |
missense variant |
R/L |
1446 |
1 |
0 |
996 |
probably damaging |
0.995 |
28001 |
likely benign |
28 |
20734 |
CCREBBP |
rs1057519884 |
SNP |
missense variant |
R/H |
1446 |
1 |
0 |
997 |
probably damaging |
0.996 |
29001 |
likely benign |
29 |
20735 |
CCREBBP |
rs398124146 |
SNP |
missense variant |
R/C |
1446 |
1 |
0 |
1000 |
probably damaging |
0.999 |
29001 |
likely benign |
29 |
20736 |
CCREBBP |
rs398124146 |
SNP |
missense variant |
R/G |
1446 |
1 |
0 |
999 |
probably damaging |
0.998 |
26001 |
likely benign |
26 |
20737 |
CCREBBP |
rs753492623 |
SNP |
missense variant |
L/V |
1445 |
1 |
0 |
986 |
probably damaging |
0.985 |
26001 |
likely benign |
26 |
20738 |
CCREBBP |
rs756756076 |
SNP |
missense variant |
R/Q |
1441 |
291 |
0.29 |
451 |
possibly damaging |
0.45 |
24001 |
likely benign |
24 |
20739 |
CCREBBP |
rs1271038944 |
SNP |
missense variant |
R/W |
1441 |
1 |
0 |
976 |
probably damaging |
0.975 |
32001 |
likely deleterious |
32 |
20740 |
CCREBBP |
rs1217572849 |
SNP |
missense variant |
I/T |
1437 |
1 |
0 |
638 |
possibly damaging |
0.637 |
25001 |
likely benign |
25 |