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 |
41651 |
APC |
rs863224541 |
SNP |
missense variant |
S/F |
1100 |
21 |
0.02 |
1 |
benign |
0 |
|
|
|
41652 |
APC |
rs878853437 |
SNP |
missense variant |
P/S |
1101 |
301 |
0.3 |
6 |
benign |
0.005 |
|
|
|
41653 |
APC |
rs1044948714 |
SNP |
missense variant |
P/L |
1101 |
1 |
0 |
111 |
benign |
0.11 |
|
|
|
41654 |
APC |
rs769608546 |
SNP |
missense variant |
Y/C |
1102 |
1 |
0 |
220 |
benign |
0.219 |
|
|
|
41655 |
APC |
rs1057521600 |
SNP |
missense variant |
R/W |
1103 |
1 |
0 |
991 |
probably damaging |
0.99 |
|
|
|
41656 |
APC |
rs200371555 |
SNP |
missense variant |
R/K |
1103 |
11 |
0.01 |
932 |
probably damaging |
0.931 |
|
|
|
41657 |
APC |
rs768454793 |
SNP |
missense variant |
R/W |
1105 |
1 |
0 |
991 |
probably damaging |
0.99 |
|
|
|
41658 |
APC |
rs548176472 |
SNP |
missense variant |
R/Q |
1105 |
1 |
0 |
969 |
probably damaging |
0.968 |
|
|
|
41659 |
APC |
rs1060503283 |
SNP |
missense variant |
A/S |
1107 |
1001 |
1 |
1 |
benign |
0 |
|
|
|
41660 |
APC |
rs151286353 |
SNP |
missense variant |
N/S |
1108 |
481 |
0.48 |
1 |
benign |
0 |
|
|
|