Disease: Liver carcinoma
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 19
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs121913409
CTNNB1
0.708 0.400 3 41224646 missense variant C/A;G;T snv 9
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
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 15
rs1057520005
TP53
0.742 0.360 17 7673800 missense variant C/A;G snv 11
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 17
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs398124146
CREBBP
0.742 0.360 16 3738617 missense variant G/A;C snv 12
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 19
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs1057519932
PIK3CA
0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057519997
TP53
0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs1057520003
TP53
0.695 0.320 17 7675996 missense variant T/G snv 20
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs121913275
PIK3CA
0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs121913412
CTNNB1
0.724 0.280 3 41224633 missense variant A/C;G;T snv 10