Disease: Squamous cell carcinoma of the head and neck
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 19
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 20
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 16
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 24
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 20
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 21
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 24
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 20
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs769696078
EGFR
0.925 0.040 7 55154128 missense variant G/A snv 3
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 21
rs745564626
XRCC3 ; KLC1
0.752 0.280 14 103699003 missense variant C/G;T snv 4.3E-05 14
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 15
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 23