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: 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: 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: 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: rs1057520030
rs1057520030
MET
7 116777427 missense variant A/G;T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.700 1.000 1 2002 2002
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
dbSNP: rs121913246
rs121913246
MET
0.827 0.200 7 116783360 missense variant A/G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.700 1.000 1 1998 1998
dbSNP: rs121913480
rs121913480
1.000 0.120 4 1806604 missense variant G/T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.700 1.000 1 2005 2005
dbSNP: rs121913482
rs121913482
0.630 0.680 4 1801837 missense variant C/T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.700 1.000 1 1999 1999
dbSNP: rs121913484
rs121913484
0.851 0.240 4 1804365 missense variant A/T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.700 1.000 1 2002 2002
dbSNP: rs121913485
rs121913485
0.716 0.400 4 1804372 missense variant A/G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.700 1.000 1 2001 2001
dbSNP: rs121913671
rs121913671
MET
0.882 0.160 7 116783353 missense variant G/A;C snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.700 1.000 1 1998 1998
dbSNP: rs28931615
rs28931615
0.732 0.240 4 1804426 missense variant C/A;T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.700 1.000 1 2009 2009
dbSNP: rs56391007
rs56391007
MET
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.700 1.000 1 1975 1975
dbSNP: rs587779383
rs587779383
0.851 0.120 4 1806157 missense variant A/C;G;T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.700 1.000 1 1998 1998
dbSNP: rs786202724
rs786202724
MET
0.925 0.120 7 116777403 missense variant G/A snv 7.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.700 1.000 1 1999 1999
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: 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: 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: rs1800566
rs1800566
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.020 1.000 2 2012 2014