Disease: Squamous cell carcinoma of the head and neck
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs375874539
TP53
0.732 0.320 17 7674237 missense variant G/A;C snv 11
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 16
rs1057519977
TP53
0.763 0.360 17 7675189 missense variant G/C snv 13
rs1057519978
TP53
0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
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
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 16
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 14
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 19
rs867262025
PIK3CA
0.790 0.360 3 179221146 missense variant G/A snv 9
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs121912655
TP53
0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs121913287
PIK3CA
0.752 0.400 3 179199088 missense variant G/A snv 11
rs121913495
GNAS
0.672 0.400 20 58909366 missense variant G/A;T snv 15
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 25