Disease: melanoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104894340
CDK4
0.827 0.200 12 57751647 missense variant C/A;T snv 5
rs1057519720
BRAF
0.851 0.080 7 140781602 missense variant CC/AA;GA mnv 4
rs1057519728
MAP2K1
0.851 0.120 15 66435103 missense variant T/A;C;G snv 5
rs1057519731
MAP2K1
0.925 0.040 15 66436816 missense variant G/C snv 2
rs1057519856
MAP2K1
0.925 0.040 15 66436815 missense variant T/A snv 2
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs121913315
STK11
0.882 0.160 19 1220488 missense variant G/A;T snv 5
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs121913361
BRAF
0.807 0.280 7 140753349 missense variant C/A;G;T snv 7
rs121913365
BRAF
0.776 0.320 7 140753332 missense variant T/A;G snv 10
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 12
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 10
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 23
rs121913407
CTNNB1
0.763 0.240 3 41224645 missense variant T/C;G snv 12
rs121913409
CTNNB1
0.708 0.400 3 41224646 missense variant C/A;G;T snv 21
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63