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 |
14151 |
SPEN |
rs771599410 |
SNP |
missense variant |
V/I |
1840 |
21 |
0.02 |
883 |
possibly damaging |
0.882 |
25001 |
likely benign |
25 |
14152 |
SPEN |
rs1161155855 |
SNP |
missense variant |
T/P |
1841 |
1 |
0 |
995 |
probably damaging |
0.994 |
26001 |
likely benign |
26 |
14153 |
SPEN |
rs777215914 |
SNP |
missense variant |
T/I |
1841 |
21 |
0.02 |
995 |
probably damaging |
0.994 |
25001 |
likely benign |
25 |
14154 |
SPEN |
rs1316034601 |
SNP |
missense variant |
R/K |
1842 |
1 |
0 |
966 |
probably damaging |
0.965 |
27001 |
likely benign |
27 |
14155 |
SPEN |
rs776167964 |
SNP |
missense variant |
E/K |
1845 |
21 |
0.02 |
872 |
possibly damaging |
0.871 |
28001 |
likely benign |
28 |
14156 |
SPEN |
rs763372934 |
SNP |
missense variant |
R/W |
1849 |
1 |
0 |
992 |
probably damaging |
0.991 |
25001 |
likely benign |
25 |
14157 |
SPEN |
rs867497648 |
SNP |
missense variant |
R/Q |
1849 |
1 |
0 |
972 |
probably damaging |
0.971 |
27001 |
likely benign |
27 |
14158 |
SPEN |
rs1277055027 |
SNP |
missense variant |
K/N |
1853 |
41 |
0.04 |
995 |
probably damaging |
0.994 |
24001 |
likely benign |
24 |
14159 |
SPEN |
rs368453661 |
SNP |
missense variant |
R/G |
1854 |
1 |
0 |
992 |
probably damaging |
0.991 |
23001 |
likely benign |
23 |
14160 |
SPEN |
rs368453661 |
SNP |
missense variant |
R/W |
1854 |
1 |
0 |
996 |
probably damaging |
0.995 |
23001 |
likely benign |
23 |