Disease: Squamous cell carcinoma of skin
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 12
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 16
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 14
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 12
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
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 15
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 17
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs28934573
TP53
0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 24
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs28934574
TP53
0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 19
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs121912657
TP53
0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 15
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19