Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912656
TP53
0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 1
rs121912657
TP53
0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 1
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 1
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 1
rs138729528
TP53
0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 1
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 1
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 1
rs28934573
TP53
0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 1
rs28934574
TP53
0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 1
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 1
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 1
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 1
rs397514495
TP53
0.882 0.120 17 7675070 missense variant C/A;T snv 1.2E-05 1
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 1
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 1
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 1
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 1
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 1
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 1
rs587782144
TP53
0.807 0.160 17 7675139 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 1
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 1
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 1
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 1
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 1
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 1