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
rs1057519718
BRAF
0.925 0.160 7 140753355 missense variant CA/TC mnv 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
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 19
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
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
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
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs12621278
ITGA6
0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 7
rs16901979
PCAT1 ; CASC19
0.724 0.480 8 127112671 intron variant C/A snv 0.16 17
rs2242652
TERT
0.724 0.400 5 1279913 intron variant G/A snv 0.18 16
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19