Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs113488022
rs113488022
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.100 1.000 23 2003 2019
dbSNP: rs121913377
rs121913377
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.100 1.000 21 2003 2019
dbSNP: rs121913483
rs121913483
0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.740 1.000 5 1999 2005
dbSNP: rs1042522
rs1042522
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.030 1.000 3 2010 2015
dbSNP: rs78311289
rs78311289
0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.710 1.000 3 1999 2001
dbSNP: rs104886003
rs104886003
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.020 1.000 2 2008 2018
dbSNP: rs1057519847
rs1057519847
0.570 0.560 7 55191821 missense variant CT/AG mnv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.020 1.000 2 2014 2015
dbSNP: rs1057519848
rs1057519848
0.570 0.560 7 55191822 missense variant TG/GT mnv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.020 1.000 2 2014 2015
dbSNP: rs121434568
rs121434568
0.568 0.560 7 55191822 missense variant T/A;G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.020 1.000 2 2014 2015
dbSNP: rs121913279
rs121913279
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.020 1.000 2 2011 2018
dbSNP: rs1463038513
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.020 1.000 2 2003 2005
dbSNP: rs1057519736
rs1057519736
0.752 0.160 15 90088605 missense variant C/G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs1057519824
rs1057519824
MET
0.807 0.120 7 116783374 missense variant T/G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.700 1.000 1 2002 2002
dbSNP: rs1057519855
rs1057519855
0.776 0.120 11 533873 missense variant CT/AC;TC mnv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs1057519883
rs1057519883
0.742 0.280 9 21971120 missense variant C/G;T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs1057520030
rs1057520030
MET
7 116777427 missense variant A/G;T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.700 1.000 1 2002 2002
dbSNP: rs1057520039
rs1057520039
0.882 0.200 19 1207169 stop gained C/G;T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs1060503115
rs1060503115
0.763 0.400 7 5978664 missense variant T/A;G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs1131691014
rs1131691014
0.439 0.800 17 7676154 frameshift variant -/C ins
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs121434265
rs121434265
0.925 0.080 1 193125142 stop gained C/G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs121912651
rs121912651
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2008 2008
dbSNP: rs121912664
rs121912664
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs121913233
rs121913233
0.627 0.520 11 533874 missense variant T/A;C;G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs121913245
rs121913245
MET
0.925 0.120 7 116783420 missense variant T/C snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.700 1.000 1 1998 1998