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 |
11061 |
MLLT4 |
rs1254753005 |
SNP |
missense variant |
T/A |
169 |
1 |
0 |
988 |
probably damaging |
0.987 |
26001 |
likely benign |
26 |
11062 |
MLLT4 |
rs139738405 |
SNP |
missense variant |
Y/D |
170 |
1 |
0 |
771 |
possibly damaging |
0.77 |
26001 |
likely benign |
26 |
11063 |
MLLT4 |
rs774439296 |
SNP |
missense variant |
V/M |
171 |
1 |
0 |
1000 |
probably damaging |
0.999 |
27001 |
likely benign |
27 |
11064 |
MLLT4 |
rs1165858456 |
SNP |
missense variant |
E/K |
172 |
31 |
0.03 |
993 |
probably damaging |
0.992 |
25001 |
likely benign |
25 |
11065 |
MLLT4 |
rs761901522 |
SNP |
missense variant |
R/G |
175 |
1 |
0 |
995 |
probably damaging |
0.994 |
27001 |
likely benign |
27 |
11066 |
MLLT4 |
rs761901522 |
SNP |
missense variant |
R/C |
175 |
1 |
0 |
999 |
probably damaging |
0.998 |
29001 |
likely benign |
29 |
11067 |
MLLT4 |
rs767822382 |
SNP |
missense variant |
R/H |
175 |
31 |
0.03 |
995 |
probably damaging |
0.994 |
24001 |
likely benign |
24 |
11068 |
MLLT4 |
rs776272198 |
SNP |
missense variant |
I/L |
176 |
31 |
0.03 |
951 |
probably damaging |
0.95 |
23001 |
likely benign |
23 |
11069 |
MLLT4 |
rs776272198 |
SNP |
missense variant |
I/V |
176 |
191 |
0.19 |
875 |
possibly damaging |
0.874 |
22001 |
likely benign |
22 |
11070 |
MLLT4 |
rs1397270661 |
SNP |
missense variant |
I/M |
176 |
1 |
0 |
997 |
probably damaging |
0.996 |
23001 |
likely benign |
23 |