Source: CLINVAR

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: rs1057519757
rs1057519757
0.882 0.120 5 68293310 missense variant G/A;C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 2 2010 2014
dbSNP: rs1057519823
rs1057519823
15 66481830 missense variant T/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 2 2009 2013
dbSNP: rs121913495
rs121913495
0.672 0.400 20 58909366 missense variant G/A;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.730 0.800 2 2010 2014
dbSNP: rs28934575
rs28934575
0.641 0.400 17 7674230 missense variant C/A;G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.740 1.000 2 2006 2018
dbSNP: rs730880502
rs730880502
15 66436762 missense variant T/A;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 2 2009 2013
dbSNP: rs104894228
rs104894228
0.605 0.560 11 534286 missense variant C/A;G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.710 1.000 1 2014 2014
dbSNP: rs1057519730
rs1057519730
1.000 0.040 15 66436786 missense variant T/A;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2009 2009
dbSNP: rs1057519816
rs1057519816
0.763 0.200 17 39711955 missense variant C/A;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.710 1.000 1 2012 2014
dbSNP: rs1057519819
rs1057519819
0.851 0.240 15 66436750 missense variant T/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2009 2009
dbSNP: rs1057519820
rs1057519820
15 66436810 missense variant A/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2009 2009
dbSNP: rs1057519821
rs1057519821
15 66436814 missense variant G/C;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2009 2009
dbSNP: rs1057519822
rs1057519822
0.925 0.080 15 66481818 missense variant T/A snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2009 2009
dbSNP: rs1057519824
rs1057519824
MET
0.807 0.120 7 116783374 missense variant T/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.710 1.000 1 2003 2007
dbSNP: rs1057519836
rs1057519836
3 41224630 missense variant A/C;G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519837
rs1057519837
1.000 0.040 3 41224631 missense variant C/G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.710 1.000 1 2011 2014
dbSNP: rs1057519838
rs1057519838
0.882 0.160 5 68293790 stop gained C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519839
rs1057519839
5 68295257 missense variant G/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519840
rs1057519840
5 68295257 inframe deletion GACAAACGTATGAACAGC/- del
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519841
rs1057519841
0.925 0.120 5 68295269 missense variant A/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519842
rs1057519842
5 68295304 inframe deletion CGA/- delins
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519843
rs1057519843
APC
5 112839522 frameshift variant AAGATTGGAAC/- del
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519844
rs1057519844
APC
5 112839522 frameshift variant AAGATTGGAACTAGGTCAGC/- del
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519845
rs1057519845
APC
5 112839990 frameshift variant GGACC/- del
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519846
rs1057519846
APC
5 112840263 frameshift variant ATTGATTC/- del
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519849
rs1057519849
8 127738386 missense variant C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014