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
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 16
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 15
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs867384286
FBXW7
0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs867262025
PIK3CA
0.790 0.360 3 179221146 missense variant G/A snv 9
rs866987936
FBXW7
0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 15
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 17
rs747241612
FBXW7
0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 12
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 14
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 12