Disease: Squamous cell carcinoma of lung
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519932
PIK3CA
0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057520003
TP53
0.695 0.320 17 7675996 missense variant T/G snv 20
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs121913272
PIK3CA
0.752 0.400 3 179210192 missense variant T/C;G snv 11
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 12
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 17
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 19
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 16
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 17
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 16
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 17
rs1057519977
TP53
0.763 0.360 17 7675189 missense variant G/C snv 13
rs747241612
FBXW7
0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs121913275
PIK3CA
0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23