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
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 15
rs869025608
MAP2K1
0.763 0.400 15 66435117 missense variant G/C;T snv 9
rs866987936
FBXW7
0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 19
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 15
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 19
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs759610249
FBXW7
0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs747241612
FBXW7
0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 17
rs398124146
CREBBP
0.742 0.360 16 3738617 missense variant G/A;C snv 12
rs397517201
PIK3CA
0.732 0.240 3 179218307 missense variant A/C;G;T snv 14
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs34968276
CDKN2A
0.776 0.240 9 21971110 stop gained G/A;C;T snv 9
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21