Disease: Liver carcinoma
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs121913281
PIK3CA
0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 17
rs121913407
CTNNB1
0.763 0.240 3 41224645 missense variant T/C;G snv 10
rs121913409
CTNNB1
0.708 0.400 3 41224646 missense variant C/A;G;T snv 9
rs121913412
CTNNB1
0.724 0.280 3 41224633 missense variant A/C;G;T snv 10
rs121913413
CTNNB1
0.763 0.240 3 41224634 missense variant C/A;T snv 9
rs121913495
GNAS
0.672 0.400 20 58909366 missense variant G/A;T snv 15
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 16
rs121913503
IDH2
0.689 0.200 15 90088606 missense variant C/A;T snv 5
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 17
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs398124146
CREBBP
0.742 0.360 16 3738617 missense variant G/A;C snv 12
rs587780071
TP53
0.732 0.240 17 7674951 missense variant G/A snv 11
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs587781991
TP53
0.724 0.240 17 7675208 missense variant C/A;T snv 14
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 19
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 15