Disease: Liver carcinoma
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 17
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs121913275
PIK3CA
0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs121913495
GNAS
0.672 0.400 20 58909366 missense variant G/A;T snv 15
rs17851045
KRAS
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 15
rs138729528
TP53
0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs1057519932
PIK3CA
0.683 0.320 3 179234298 missense variant T/G snv 22
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 17
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs11554273
GNAS
0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 17
rs121913503
IDH2
0.689 0.200 15 90088606 missense variant C/A;T snv 5
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs1057520003
TP53
0.695 0.320 17 7675996 missense variant T/G snv 20
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 17
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 19