Disease: Non-Small Cell Lung Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1026411
LOC105375751 ; PCAT1
0.827 0.080 8 127014165 intron variant G/A;C snv 0.25 5
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1051753269
EGFR
0.790 0.120 7 55174029 missense variant G/A snv 7.0E-06 7
rs1057519698
ALK
0.827 0.120 2 29222347 missense variant A/G;T snv 8
rs1057519729
MAP2K1
0.827 0.080 15 66435113 missense variant A/C snv 6
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1057519861
EGFR ; EGFR-AS1
0.776 0.080 7 55181398 missense variant T/A snv 15
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs10680577
RAB4B-EGLN2 ; EGLN2
0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs1171287261
EGFR
0.851 0.080 7 55191839 missense variant G/A snv 4
rs11778573
CCN4
0.851 0.080 8 133216687 intron variant T/G snv 0.59 4
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs121913465
EGFR ; EGFR-AS1
0.763 0.160 7 55181312 missense variant G/T snv 11
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63