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 |
7761 |
KM2TC-MLL3 |
rs751148559 |
SNP |
missense variant |
S/N |
3124 |
1001 |
1 |
1 |
benign |
0 |
14001 |
likely benign |
14 |
7762 |
KM2TC-MLL3 |
rs1244312926 |
SNP |
missense variant |
V/L |
3122 |
1 |
0 |
985 |
probably damaging |
0.984 |
25001 |
likely benign |
25 |
7763 |
KM2TC-MLL3 |
rs1244312926 |
SNP |
missense variant |
V/M |
3122 |
1 |
0 |
999 |
probably damaging |
0.998 |
25001 |
likely benign |
25 |
7764 |
KM2TC-MLL3 |
rs1049142169 |
SNP |
missense variant |
M/I |
3121 |
81 |
0.08 |
938 |
probably damaging |
0.937 |
24001 |
likely benign |
24 |
7765 |
KM2TC-MLL3 |
rs945132538 |
SNP |
missense variant |
M/V |
3121 |
41 |
0.04 |
938 |
probably damaging |
0.937 |
24001 |
likely benign |
24 |
7766 |
KM2TC-MLL3 |
rs368317084 |
SNP |
missense variant |
P/L |
3120 |
1 |
0 |
999 |
probably damaging |
0.998 |
31001 |
likely deleterious |
31 |
7767 |
KM2TC-MLL3 |
rs1172944883 |
SNP |
missense variant |
P/S |
3120 |
31 |
0.03 |
998 |
probably damaging |
0.997 |
24001 |
likely benign |
24 |
7768 |
KM2TC-MLL3 |
rs766962867 |
SNP |
missense variant |
M/T |
3118 |
1 |
0 |
943 |
probably damaging |
0.942 |
26001 |
likely benign |
26 |
7769 |
KM2TC-MLL3 |
rs750388935 |
SNP |
missense variant |
M/V |
3118 |
141 |
0.14 |
915 |
probably damaging |
0.914 |
23001 |
likely benign |
23 |
7770 |
KM2TC-MLL3 |
rs577646181 |
SNP |
missense variant |
G/D |
3117 |
1 |
0 |
1000 |
probably damaging |
0.999 |
25001 |
likely benign |
25 |