Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 1
rs28934573
TP53
0.667 0.480 17 7674241 missense variant G/A;C;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
rs121913495
GNAS
0.672 0.400 20 58909366 missense variant G/A;T snv 2
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 2
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 1
rs138729528
TP53
0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 1
rs1057519925
PIK3CA
0.683 0.560 3 179210291 missense variant G/A;C snv 1
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 1
rs121912657
TP53
0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 1
rs371769427
U2AF1
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 1
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 1
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 1
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 1
rs11554273
GNAS
0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 1
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 1
rs28931589
CTNNB1
0.695 0.240 3 41224613 missense variant G/A;C;T snv 1
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 1
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 1
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 1
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 1
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 1
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 1
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 1
rs121913502
IDH2
0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 1