Disease: Renal Cell Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519932
PIK3CA
0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057519977
TP53
0.763 0.360 17 7675189 missense variant G/C snv 13
rs1057519978
TP53
0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057520003
TP53
0.695 0.320 17 7675996 missense variant T/G snv 20
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 21
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
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
rs121913281
PIK3CA
0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 16
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 22
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 20
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs28934573
TP53
0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 28
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 23