Disease: Esophageal carcinoma
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 16
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 14
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 17
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 19
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 15
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 19
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 15
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 16