Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.47412570_47415848delCA331682MSH2c.792+10_943-448del
c.594+10_745-448del
n.864+10_1015-448del
n.854+10_1005-448del
 ClinVar
2g.47414261A=CA2495833731MSH2c.793-8A= (n.793-8A=)
c.595-8A= (n.595-8A=)
n.865-8A=
n.855-8A=
2g.47414261A>CCA1139656927MSH2c.793-8A>C (n.793-8A>C)
c.595-8A>C (n.595-8A>C)
n.865-8A>C
n.855-8A>C
 ClinVar dbSNP gnomAD v4
2g.47414261A>GCA2658946479MSH2c.793-8A>G (n.793-8A>G)
c.595-8A>G (n.595-8A>G)
n.865-8A>G
n.855-8A>G
 gnomAD v4
2g.47414261A>TCA2699139486MSH2c.793-8A>T (n.793-8A>T)
c.595-8A>T (n.595-8A>T)
n.865-8A>T
n.855-8A>T
 dbSNP
2g.47414262_47414868delinsATTTTAGGTTGCAGTTTCATCACTGTCTGCGGTAATCAAGTTTTTAGAACTCTTATCAGATGATTCCAACTTTGGACAGTTTGAACTGACTACTTTTGACTTCAGCCAGTATATGAAATTGGATATTGCAGCAGTCAGAGCCCTTAACCTTTTTCAGGTAAAAAAAAAAAAAAAAAAAAAAAAAAAGGGTTAAAAATGTTGAATGGTTAAAAAATGTTTTCATTGACATATACTGAAGAAGCTTATAAAGGAGCTAAAATATTTTGAAATATTATTATACTTGGATTAGATAACTAGCTTTAAATGGCTGTATTTTTCTCTCCCCTCCTCCACTCCACTTTTTAACTTTTTTTTTTTTAAGTCAGAGTCTCACTTGTTCCCTAGGCCAGAGTGCAGTGGCACAATCTCAGCCCACTCTAACCTCCACCTCCCAAGTAGTTGGGATTACAGTTGCCTGCCACCATGCCTGGTTAATTTTTATATTTTTAGTAGGGTTGCGGGGACAGGGTTTCACCATGTTGGCCAGGTTGGTCTCAAACTTCTGACCTTAGGTGATCCTCCCACCTCGGCTTCCCAAAGTGCTGGGATTACAGGCTTGAGCCATCGTCA2495833736MSH2c.793-7_942+450delinsATTTTAGGTTGCAGTTTCATCACTGTCTGCGGTAATCAAGTTTTTAGAACTCTTATCAGATGATTCCAACTTTGGACAGTTTGAACTGACTACTTTTGACTTCAGCCAGTATATGAAATTGGATATTGCAGCAGTCAGAGCCCTTAACCTTTTTCAGGTAAAAAAAAAAAAAAAAAAAAAAAAAAAGGGTTAAAAATGTTGAATGGTTAAAAAATGTTTTCATTGACATATACTGAAGAAGCTTATAAAGGAGCTAAAATATTTTGAAATATTATTATACTTGGATTAGATAACTAGCTTTAAATGGCTGTATTTTTCTCTCCCCTCCTCCACTCCACTTTTTAACTTTTTTTTTTTTAAGTCAGAGTCTCACTTGTTCCCTAGGCCAGAGTGCAGTGGCACAATCTCAGCCCACTCTAACCTCCACCTCCCAAGTAGTTGGGATTACAGTTGCCTGCCACCATGCCTGGTTAATTTTTATATTTTTAGTAGGGTTGCGGGGACAGGGTTTCACCATGTTGGCCAGGTTGGTCTCAAACTTCTGACCTTAGGTGATCCTCCCACCTCGGCTTCCCAAAGTGCTGGGATTACAGGCTTGAGCCATCGT
c.595-7_744+450delinsATTTTAGGTTGCAGTTTCATCACTGTCTGCGGTAATCAAGTTTTTAGAACTCTTATCAGATGATTCCAACTTTGGACAGTTTGAACTGACTACTTTTGACTTCAGCCAGTATATGAAATTGGATATTGCAGCAGTCAGAGCCCTTAACCTTTTTCAGGTAAAAAAAAAAAAAAAAAAAAAAAAAAAGGGTTAAAAATGTTGAATGGTTAAAAAATGTTTTCATTGACATATACTGAAGAAGCTTATAAAGGAGCTAAAATATTTTGAAATATTATTATACTTGGATTAGATAACTAGCTTTAAATGGCTGTATTTTTCTCTCCCCTCCTCCACTCCACTTTTTAACTTTTTTTTTTTTAAGTCAGAGTCTCACTTGTTCCCTAGGCCAGAGTGCAGTGGCACAATCTCAGCCCACTCTAACCTCCACCTCCCAAGTAGTTGGGATTACAGTTGCCTGCCACCATGCCTGGTTAATTTTTATATTTTTAGTAGGGTTGCGGGGACAGGGTTTCACCATGTTGGCCAGGTTGGTCTCAAACTTCTGACCTTAGGTGATCCTCCCACCTCGGCTTCCCAAAGTGCTGGGATTACAGGCTTGAGCCATCGT
n.865-7_1014+450delinsATTTTAGGTTGCAGTTTCATCACTGTCTGCGGTAATCAAGTTTTTAGAACTCTTATCAGATGATTCCAACTTTGGACAGTTTGAACTGACTACTTTTGACTTCAGCCAGTATATGAAATTGGATATTGCAGCAGTCAGAGCCCTTAACCTTTTTCAGGTAAAAAAAAAAAAAAAAAAAAAAAAAAAGGGTTAAAAATGTTGAATGGTTAAAAAATGTTTTCATTGACATATACTGAAGAAGCTTATAAAGGAGCTAAAATATTTTGAAATATTATTATACTTGGATTAGATAACTAGCTTTAAATGGCTGTATTTTTCTCTCCCCTCCTCCACTCCACTTTTTAACTTTTTTTTTTTTAAGTCAGAGTCTCACTTGTTCCCTAGGCCAGAGTGCAGTGGCACAATCTCAGCCCACTCTAACCTCCACCTCCCAAGTAGTTGGGATTACAGTTGCCTGCCACCATGCCTGGTTAATTTTTATATTTTTAGTAGGGTTGCGGGGACAGGGTTTCACCATGTTGGCCAGGTTGGTCTCAAACTTCTGACCTTAGGTGATCCTCCCACCTCGGCTTCCCAAAGTGCTGGGATTACAGGCTTGAGCCATCGT
n.855-7_1004+450delinsATTTTAGGTTGCAGTTTCATCACTGTCTGCGGTAATCAAGTTTTTAGAACTCTTATCAGATGATTCCAACTTTGGACAGTTTGAACTGACTACTTTTGACTTCAGCCAGTATATGAAATTGGATATTGCAGCAGTCAGAGCCCTTAACCTTTTTCAGGTAAAAAAAAAAAAAAAAAAAAAAAAAAAGGGTTAAAAATGTTGAATGGTTAAAAAATGTTTTCATTGACATATACTGAAGAAGCTTATAAAGGAGCTAAAATATTTTGAAATATTATTATACTTGGATTAGATAACTAGCTTTAAATGGCTGTATTTTTCTCTCCCCTCCTCCACTCCACTTTTTAACTTTTTTTTTTTTAAGTCAGAGTCTCACTTGTTCCCTAGGCCAGAGTGCAGTGGCACAATCTCAGCCCACTCTAACCTCCACCTCCCAAGTAGTTGGGATTACAGTTGCCTGCCACCATGCCTGGTTAATTTTTATATTTTTAGTAGGGTTGCGGGGACAGGGTTTCACCATGTTGGCCAGGTTGGTCTCAAACTTCTGACCTTAGGTGATCCTCCCACCTCGGCTTCCCAAAGTGCTGGGATTACAGGCTTGAGCCATCGT
2g.47414263T>ACA2699275104MSH2c.793-6T>A (n.793-6T>A)
c.595-6T>A (n.595-6T>A)
n.865-6T>A
n.855-6T>A
 dbSNP
2g.47414263T>CCA2697548096MSH2c.793-6T>C (n.793-6T>C)
c.595-6T>C (n.595-6T>C)
n.865-6T>C
n.855-6T>C
 ClinVar dbSNP
2g.47414263_47414868delCA331685MSH2c.793-6_942+450del
c.595-6_744+450del
n.865-6_1014+450del
n.855-6_1004+450del
 ClinVar dbSNP
2g.47414264T>CCA2699275123MSH2c.793-5T>C (n.793-5T>C)
c.595-5T>C (n.595-5T>C)
n.865-5T>C
n.855-5T>C
 dbSNP
2g.47414265T>CCA2699275126MSH2c.793-4T>C (n.793-4T>C)
c.595-4T>C (n.595-4T>C)
n.865-4T>C
n.855-4T>C
 ClinVar dbSNP
2g.47414267_47416282delCA2499216016MSH2c.793-2_943-14del
c.595-2_745-14del
n.865-2_1015-14del
n.855-2_1005-14del
 ClinVar
2g.47414266T>CCA913187991MSH2c.793-3T>C (n.793-3T>C)
c.595-3T>C (n.595-3T>C)
n.865-3T>C
n.855-3T>C
 ClinVar dbSNP
2g.47414266T=CA2495833741MSH2c.793-3T= (n.793-3T=)
c.595-3T= (n.595-3T=)
n.865-3T=
n.855-3T=
2g.47414267A=CA2495833747MSH2c.793-2A= (n.793-2A=)
c.595-2A= (n.595-2A=)
n.865-2A=
n.855-2A=
2g.47414267A>CCA022304MSH2c.793-2A>C (n.793-2A>C)
c.595-2A>C (n.595-2A>C)
n.865-2A>C
n.855-2A>C
 ClinVar dbSNP
2g.47414267A>GCA346732732MSH2c.793-2A>G (n.793-2A>G)
c.595-2A>G (n.595-2A>G)
n.865-2A>G
n.855-2A>G
 ClinVar dbSNP gnomAD v4
2g.47414267A>TCA346732733MSH2c.793-2A>T (n.793-2A>T)
c.595-2A>T (n.595-2A>T)
n.865-2A>T
n.855-2A>T
 ClinVar dbSNP
2g.47414267_47414268insAAATTAACA1139771894MSH2c.793-2_793-1insAAATTAA (n.793-2_793-1insAAATTAA)
c.595-2_595-1insAAATTAA (n.595-2_595-1insAAATTAA)
n.865-2_865-1insAAATTAA
n.855-2_855-1insAAATTAA
2g.47414267_47414272delinsAGGTTGCA2495833751MSH2c.793-2_796delinsAGGTTG
c.595-2_598delinsAGGTTG
n.865-2_868delinsAGGTTG
n.855-2_858delinsAGGTTG
2g.47414268G>ACA279694MSH2c.793-1G>A (n.793-1G>A)
c.595-1G>A (n.595-1G>A)
n.865-1G>A
n.855-1G>A
 ClinVar dbSNP
2g.47414268G>CCA346732734MSH2c.793-1G>C (n.793-1G>C)
c.595-1G>C (n.595-1G>C)
n.865-1G>C
n.855-1G>C
 ClinVar dbSNP
2g.47414268G=CA2495833758MSH2c.793-1G= (n.793-1G=)
c.595-1G= (n.595-1G=)
n.865-1G=
n.855-1G=
2g.47414268G>TCA346732735MSH2c.793-1G>T (n.793-1G>T)
c.595-1G>T (n.595-1G>T)
n.865-1G>T
n.855-1G>T
 ClinVar dbSNP
2g.47414268_47414269delCA1139771123MSH2c.793-1_793del
c.595-1_595del
n.865-1_865del
n.855-1_855del
2g.47414268_47414272delCA2573051956MSH2c.793-1_796del
c.595-1_598del
n.865-1_868del
n.855-1_858del
 dbSNP
2g.47414268_47414272delinsAAATTAAGACA273851MSH2c.793-1_796delinsAAATTAAGA
c.595-1_598delinsAAATTAAGA
n.865-1_868delinsAAATTAAGA
n.855-1_858delinsAAATTAAGA
 dbSNP
2g.47414269G>ACA346732737MSH2c.793G>A (p.Val265Ile)
c.595G>A (p.Val199Ile)
n.865G>A
n.855G>A
 ClinVar dbSNP
2g.47414269G>CCA346732738MSH2c.793G>C (p.Val265Leu)
c.595G>C (p.Val199Leu)
n.865G>C
n.855G>C
 dbSNP
2g.47414269G=CA2495833762MSH2c.793G= (p.Val265=)
c.595G= (p.Val199=)
n.865G=
n.855G=
2g.47414269G>TCA346732736MSH2c.793G>T (p.Val265Phe)
c.595G>T (p.Val199Phe)
n.865G>T
n.855G>T
 ClinVar dbSNP gnomAD v4
2g.47414269_47414270delinsGTCA2495833763MSH2c.793_794delinsGT (p.Val265=)
c.595_596delinsGT (p.Val199=)
n.865_866delinsGT
n.855_856delinsGT
2g.47414269_47414270insAAACA1139532100MSH2c.793_794insAAA (p.Val265delinsGluIle)
c.595_596insAAA (p.Val199delinsGluIle)
n.865_866insAAA
n.855_856insAAA
2g.47414270T>ACA346732739MSH2c.794T>A (p.Val265Asp)
c.596T>A (p.Val199Asp)
n.866T>A
n.856T>A
 dbSNP
2g.47414270T>CCA346732740MSH2c.794T>C (p.Val265Ala)
c.596T>C (p.Val199Ala)
n.866T>C
n.856T>C
 dbSNP
2g.47414270T>GCA346732741MSH2c.794T>G (p.Val265Gly)
c.596T>G (p.Val199Gly)
n.866T>G
n.856T>G
2g.47414271delCA022317MSH2c.795del (p.Ala266GlnfsTer8)
c.597del (p.Ala200GlnfsTer8)
n.867del
n.857del
 ClinVar dbSNP
2g.47414271T>ACA425969588MSH2c.795T>A (p.Val265=)
c.597T>A (p.Val199=)
n.867T>A
n.857T>A
2g.47414271T>CCA022323MSH2c.795T>C (p.Val265=)
c.597T>C (p.Val199=)
n.867T>C
n.857T>C
 dbSNP
2g.47414271T>GCA040664MSH2c.795T>G (p.Val265=)
c.597T>G (p.Val199=)
n.867T>G
n.857T>G
 ClinVar dbSNP ExAC gnomAD v2
2g.47414271T=CA2495833766MSH2c.795T= (p.Val265=)
c.597T= (p.Val199=)
n.867T=
n.857T=
2g.47414272delCA2699275188MSH2c.796del (p.Ala266GlnfsTer8)
c.598del (p.Ala200GlnfsTer8)
n.868del
n.858del
 dbSNP
2g.47414272G>ACA346732742MSH2c.796G>A (p.Ala266Thr)
c.598G>A (p.Ala200Thr)
n.868G>A
n.858G>A
 ClinVar dbSNP
2g.47414272G>CCA346732743MSH2c.796G>C (p.Ala266Pro)
c.598G>C (p.Ala200Pro)
n.868G>C
n.858G>C
 dbSNP
2g.47414272G=CA2495833769MSH2c.796G= (p.Ala266=)
c.598G= (p.Ala200=)
n.868G=
n.858G=
2g.47414272G>TCA346732744MSH2c.796G>T (p.Ala266Ser)
c.598G>T (p.Ala200Ser)
n.868G>T
n.858G>T
 dbSNP gnomAD v4
2g.47414272_47414273delCA2580066979MSH2c.796_797del (p.Ala266SerfsTer17)
c.598_599del (p.Ala200SerfsTer17)
n.868_869del
n.858_859del
 ClinVar
2g.47414273C>ACA346732745MSH2c.797C>A (p.Ala266Glu)
c.599C>A (p.Ala200Glu)
n.869C>A
n.859C>A
 ClinVar dbSNP COSMIC
2g.47414273C=CA2495833775MSH2c.797C= (p.Ala266=)
c.599C= (p.Ala200=)
n.869C=
n.859C=
2g.47414273C>GCA346732746MSH2c.797C>G (p.Ala266Gly)
c.599C>G (p.Ala200Gly)
n.869C>G
n.859C>G
2g.47414273C>TCA022328MSH2c.797C>T (p.Ala266Val)
c.599C>T (p.Ala200Val)
n.869C>T
n.859C>T
 ClinVar dbSNP
2g.47414274A=CA2495833782MSH2c.798A= (p.Ala266=)
c.600A= (p.Ala200=)
n.870A=
n.860A=
2g.47414274A>CCA425969607MSH2c.798A>C (p.Ala266=)
c.600A>C (p.Ala200=)
n.870A>C
n.860A>C
2g.47414274A>GCA425969610MSH2c.798A>G (p.Ala266=)
c.600A>G (p.Ala200=)
n.870A>G
n.860A>G
 ClinVar dbSNP
2g.47414274A>TCA10582004MSH2c.798A>T (p.Ala266=)
c.600A>T (p.Ala200=)
n.870A>T
n.860A>T
 ClinVar dbSNP
2g.47414275G>ACA346732749MSH2c.799G>A (p.Val267Ile)
c.601G>A (p.Val201Ile)
n.871G>A
n.861G>A
 ClinVar dbSNP COSMIC
2g.47414275G>CCA346732748MSH2c.799G>C (p.Val267Leu)
c.601G>C (p.Val201Leu)
n.871G>C
n.861G>C
 ClinVar dbSNP
2g.47414275G>TCA346732747MSH2c.799G>T (p.Val267Phe)
c.601G>T (p.Val201Phe)
n.871G>T
n.861G>T
 ClinVar
2g.47414276T>ACA346732750MSH2c.800T>A (p.Val267Asp)
c.602T>A (p.Val201Asp)
n.872T>A
n.862T>A
2g.47414276T>CCA346732751MSH2c.800T>C (p.Val267Ala)
c.602T>C (p.Val201Ala)
n.872T>C
n.862T>C
2g.47414276T>GCA346732752MSH2c.800T>G (p.Val267Gly)
c.602T>G (p.Val201Gly)
n.872T>G
n.862T>G
2g.47414278dupCA2580066987MSH2c.802dup (p.Ser268PhefsTer16)
c.604dup (p.Ser202PhefsTer16)
n.874dup
n.864dup
 ClinVar
2g.47414278delCA2580066986MSH2c.802del (p.Ser268HisfsTer6)
c.604del (p.Ser202HisfsTer6)
n.874del
n.864del
 ClinVar
2g.47414278_47414315delCA2580066985MSH2c.802_839del (p.Ser268IlefsTer3)
c.604_641del (p.Ser202IlefsTer3)
n.874_911del
n.864_901del
 ClinVar
2g.47414277T>ACA425969630MSH2c.801T>A (p.Val267=)
c.603T>A (p.Val201=)
n.873T>A
n.863T>A
 dbSNP COSMIC
2g.47414277T>CCA425969628MSH2c.801T>C (p.Val267=)
c.603T>C (p.Val201=)
n.873T>C
n.863T>C
2g.47414277T>GCA425969626MSH2c.801T>G (p.Val267=)
c.603T>G (p.Val201=)
n.873T>G
n.863T>G
 ClinVar dbSNP
2g.47414278_47414289dupCA2580066989MSH2c.802_813dup (p.Ser271_Ala272insSerSerLeuSer)
c.604_615dup (p.Ser205_Ala206insSerSerLeuSer)
n.874_885dup
n.864_875dup
 ClinVar
2g.47414278T>ACA346732753MSH2c.802T>A (p.Ser268Thr)
c.604T>A (p.Ser202Thr)
n.874T>A
n.864T>A
2g.47414278T>CCA346732754MSH2c.802T>C (p.Ser268Pro)
c.604T>C (p.Ser202Pro)
n.874T>C
n.864T>C
 dbSNP
2g.47414278T>GCA10577951MSH2c.802T>G (p.Ser268Ala)
c.604T>G (p.Ser202Ala)
n.874T>G
n.864T>G
 ClinVar dbSNP gnomAD v4
2g.47414278T=CA2495833786MSH2c.802T= (p.Ser268=)
c.604T= (p.Ser202=)
n.874T=
n.864T=
2g.47414278_47414279insGTCA2582342372MSH2c.802_803insGT (p.Ser268CysfsTer7)
c.604_605insGT (p.Ser202CysfsTer7)
n.874_875insGT
n.864_865insGT
 ClinVar
2g.47414279C>ACA346732755MSH2c.803C>A (p.Ser268Ter)
c.605C>A (p.Ser202Ter)
n.875C>A
n.865C>A
 ClinVar dbSNP
2g.47414279C=CA2495833795MSH2c.803C= (p.Ser268=)
c.605C= (p.Ser202=)
n.875C=
n.865C=
2g.47414279C>GCA346732756MSH2c.803C>G (p.Ser268Ter)
c.605C>G (p.Ser202Ter)
n.875C>G
n.865C>G
 ClinVar dbSNP
2g.47414279C>TCA040677MSH2c.803C>T (p.Ser268Leu)
c.605C>T (p.Ser202Leu)
n.875C>T
n.865C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47414280A=CA2495833804MSH2c.804A= (p.Ser268=)
c.606A= (p.Ser202=)
n.876A=
n.866A=
2g.47414280A>CCA425969645MSH2c.804A>C (p.Ser268=)
c.606A>C (p.Ser202=)
n.876A>C
n.866A>C
2g.47414280A>GCA16604138MSH2c.804A>G (p.Ser268=)
c.606A>G (p.Ser202=)
n.876A>G
n.866A>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.47414280A>TCA10577952MSH2c.804A>T (p.Ser268=)
c.606A>T (p.Ser202=)
n.876A>T
n.866A>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47414280dupCA2586969209MSH2c.804dup (p.Ser269IlefsTer15)
c.606dup (p.Ser203IlefsTer15)
n.876dup
n.866dup
2g.47414281T>ACA346732757MSH2c.805T>A (p.Ser269Thr)
c.607T>A (p.Ser203Thr)
n.877T>A
n.867T>A
2g.47414281T>CCA346732758MSH2c.805T>C (p.Ser269Pro)
c.607T>C (p.Ser203Pro)
n.877T>C
n.867T>C
 dbSNP
2g.47414281T>GCA346732759MSH2c.805T>G (p.Ser269Ala)
c.607T>G (p.Ser203Ala)
n.877T>G
n.867T>G
2g.47414282C>ACA16042056MSH2c.806C>A (p.Ser269Ter)
c.608C>A (p.Ser203Ter)
n.878C>A
n.868C>A
 ClinVar dbSNP
2g.47414282C=CA2495833811MSH2c.806C= (p.Ser269=)
c.608C= (p.Ser203=)
n.878C=
n.868C=
2g.47414282C>GCA346732760MSH2c.806C>G (p.Ser269Ter)
c.608C>G (p.Ser203Ter)
n.878C>G
n.868C>G
 ClinVar dbSNP
2g.47414282C>TCA022333MSH2c.806C>T (p.Ser269Leu)
c.608C>T (p.Ser203Leu)
n.878C>T
n.868C>T
 ClinVar dbSNP
2g.47414282_47414283insTGTACCGCAGATTCA16617565MSH2c.806_807insTGTACCGCAGATT (p.Leu270ValfsTer18)
c.608_609insTGTACCGCAGATT (p.Leu204ValfsTer18)
n.878_879insTGTACCGCAGATT
n.868_869insTGTACCGCAGATT
 ClinVar dbSNP
2g.47414283A>CCA425969666MSH2c.807A>C (p.Ser269=)
c.609A>C (p.Ser203=)
n.879A>C
n.869A>C
2g.47414283A>GCA425969661MSH2c.807A>G (p.Ser269=)
c.609A>G (p.Ser203=)
n.879A>G
n.869A>G
 ClinVar dbSNP
2g.47414283A>TCA425969664MSH2c.807A>T (p.Ser269=)
c.609A>T (p.Ser203=)
n.879A>T
n.869A>T
 dbSNP
2g.47414283dupCA46683826MSH2c.807dup (p.Leu270ThrfsTer14)
c.609dup (p.Leu204ThrfsTer14)
n.879dup
n.869dup
 dbSNP
2g.47414283_47414287delinsACTGTCA2495833818MSH2c.807_811delinsACTGT (p.Ser269=)
c.609_613delinsACTGT (p.Ser203=)
n.879_883delinsACTGT
n.869_873delinsACTGT
2g.47414284C>ACA346732761MSH2c.808C>A (p.Leu270Met)
c.610C>A (p.Leu204Met)
n.880C>A
n.870C>A
 dbSNP
2g.47414284C=CA2495833827MSH2c.808C= (p.Leu270=)
c.610C= (p.Leu204=)
n.880C=
n.870C=
2g.47414284C>GCA040694MSH2c.808C>G (p.Leu270Val)
c.610C>G (p.Leu204Val)
n.880C>G
n.870C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47414284C>TCA425969674MSH2c.808C>T (p.Leu270=)
c.610C>T (p.Leu204=)
n.880C>T
n.870C>T
 ClinVar dbSNP
2g.47414284_47414286delinsCTGCA2495833826MSH2c.808_810delinsCTG (p.Leu270=)
c.610_612delinsCTG (p.Leu204=)
n.880_882delinsCTG
n.870_872delinsCTG
2g.47414287_47414290delCA022348MSH2c.811_814del (p.Ser271ArgfsTer2)
c.613_616del (p.Ser205ArgfsTer2)
n.883_886del
n.873_876del
 ClinVar dbSNP
2g.47414285T>ACA346732762MSH2c.809T>A (p.Leu270Gln)
c.611T>A (p.Leu204Gln)
n.881T>A
n.871T>A
2g.47414285T>CCA346732763MSH2c.809T>C (p.Leu270Pro)
c.611T>C (p.Leu204Pro)
n.881T>C
n.871T>C
 ClinVar dbSNP
2g.47414285T>GCA346732764MSH2c.809T>G (p.Leu270Arg)
c.611T>G (p.Leu204Arg)
n.881T>G
n.871T>G
 ClinVar
2g.47414285T=CA2495833834MSH2c.809T= (p.Leu270=)
c.611T= (p.Leu204=)
n.881T=
n.871T=
2g.47414286_47414287delCA022343MSH2c.810_811del (p.Ser271CysfsTer12)
c.612_613del (p.Ser205CysfsTer12)
n.882_883del
n.872_873del
 ClinVar dbSNP
2g.47414286G>ACA425969691MSH2c.810G>A (p.Leu270=)
c.612G>A (p.Leu204=)
n.882G>A
n.872G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47414286G>CCA425969694MSH2c.810G>C (p.Leu270=)
c.612G>C (p.Leu204=)
n.882G>C
n.872G>C
 ClinVar dbSNP
2g.47414286G=CA2495833841MSH2c.810G= (p.Leu270=)
c.612G= (p.Leu204=)
n.882G=
n.872G=
2g.47414286G>TCA10577953MSH2c.810G>T (p.Leu270=)
c.612G>T (p.Leu204=)
n.882G>T
n.872G>T
 ClinVar dbSNP
2g.47414286_47414288delinsGTCCA2495833839MSH2c.810_812delinsGTC (p.Leu270=)
c.612_614delinsGTC (p.Leu204=)
n.882_884delinsGTC
n.872_874delinsGTC
2g.47414287T>ACA346732765MSH2c.811T>A (p.Ser271Thr)
c.613T>A (p.Ser205Thr)
n.883T>A
n.873T>A
2g.47414287T>CCA346732767MSH2c.811T>C (p.Ser271Pro)
c.613T>C (p.Ser205Pro)
n.883T>C
n.873T>C
2g.47414287T>GCA346732766MSH2c.811T>G (p.Ser271Ala)
c.613T>G (p.Ser205Ala)
n.883T>G
n.873T>G
2g.47414288_47414289delCA915943890MSH2c.812_813del (p.Ser271CysfsTer12)
c.614_615del (p.Ser205CysfsTer12)
n.884_885del
n.874_875del
 ClinVar dbSNP
2g.47414287_47414290delinsCTGTCA46683881MSH2c.811_814delinsCTGT (p.Ser271_Ala272delinsLeuSer)
c.613_616delinsCTGT (p.Ser205_Ala206delinsLeuSer)
n.883_886delinsCTGT
n.873_876delinsCTGT
2g.47414287_47414290delinsGTCTCA46683885MSH2c.811_814delinsGTCT (p.Ser271_Ala272delinsValSer)
c.613_616delinsGTCT (p.Ser205_Ala206delinsValSer)
n.883_886delinsGTCT
n.873_876delinsGTCT
2g.47414288C>ACA10577954MSH2c.812C>A (p.Ser271Tyr)
c.614C>A (p.Ser205Tyr)
n.884C>A
n.874C>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47414288C=CA2495833850MSH2c.812C= (p.Ser271=)
c.614C= (p.Ser205=)
n.884C=
n.874C=
2g.47414288C>GCA349912MSH2c.812C>G (p.Ser271Cys)
c.614C>G (p.Ser205Cys)
n.884C>G
n.874C>G
 ClinVar dbSNP gnomAD v4
2g.47414288C>TCA46683893MSH2c.812C>T (p.Ser271Phe)
c.614C>T (p.Ser205Phe)
n.884C>T
n.874C>T
 ClinVar dbSNP
2g.47414289T>ACA425969710MSH2c.813T>A (p.Ser271=)
c.615T>A (p.Ser205=)
n.885T>A
n.875T>A
2g.47414289T>CCA425969712MSH2c.813T>C (p.Ser271=)
c.615T>C (p.Ser205=)
n.885T>C
n.875T>C
 ClinVar dbSNP
2g.47414289T>GCA16604229MSH2c.813T>G (p.Ser271=)
c.615T>G (p.Ser205=)
n.885T>G
n.875T>G
 ClinVar dbSNP
2g.47414289T=CA2495833858MSH2c.813T= (p.Ser271=)
c.615T= (p.Ser205=)
n.885T=
n.875T=
2g.47414290G>ACA346732768MSH2c.814G>A (p.Ala272Thr)
c.616G>A (p.Ala206Thr)
n.886G>A
n.876G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47414290G>CCA346732770MSH2c.814G>C (p.Ala272Pro)
c.616G>C (p.Ala206Pro)
n.886G>C
n.876G>C
 dbSNP
2g.47414290G=CA2495833874MSH2c.814G= (p.Ala272=)
c.616G= (p.Ala206=)
n.886G=
n.876G=
2g.47414290G>TCA346732769MSH2c.814G>T (p.Ala272Ser)
c.616G>T (p.Ala206Ser)
n.886G>T
n.876G>T
2g.47414290_47414291delinsATCA022352MSH2c.814_815delinsAT (p.Ala272Met)
c.616_617delinsAT (p.Ala206Met)
n.886_887delinsAT
n.876_877delinsAT
 dbSNP
2g.47414290_47414291delinsGCCA2495833864MSH2c.814_815delinsGC (p.Ala272=)
c.616_617delinsGC (p.Ala206=)
n.886_887delinsGC
n.876_877delinsGC
2g.47414291C>ACA346732771MSH2c.815C>A (p.Ala272Glu)
c.617C>A (p.Ala206Glu)
n.887C>A
n.877C>A
 dbSNP
2g.47414291C=CA2495833884MSH2c.815C= (p.Ala272=)
c.617C= (p.Ala206=)
n.887C=
n.877C=
2g.47414291C>GCA346732772MSH2c.815C>G (p.Ala272Gly)
c.617C>G (p.Ala206Gly)
n.887C>G
n.877C>G
 dbSNP
2g.47414291C>TCA022356MSH2c.815C>T (p.Ala272Val)
c.617C>T (p.Ala206Val)
n.887C>T
n.877C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47414291_47414292delinsCGCA2495833882MSH2c.815_816delinsCG (p.Ala272=)
c.617_618delinsCG (p.Ala206=)
n.887_888delinsCG
n.877_878delinsCG
2g.47414292G>ACA040753MSH2c.816G>A (p.Ala272=)
c.618G>A (p.Ala206=)
n.888G>A
n.878G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47414292G>CCA425969726MSH2c.816G>C (p.Ala272=)
c.618G>C (p.Ala206=)
n.888G>C
n.878G>C
 ClinVar
2g.47414292G=CA2495833893MSH2c.816G= (p.Ala272=)
c.618G= (p.Ala206=)
n.888G=
n.878G=
2g.47414292G>TCA425969723MSH2c.816G>T (p.Ala272=)
c.618G>T (p.Ala206=)
n.888G>T
n.878G>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.47414293delCA1139656931MSH2c.817del (p.Val273Ter)
c.619del (p.Val207Ter)
n.889del
n.879del
 ClinVar dbSNP
2g.47414293G>ACA040766MSH2c.817G>A (p.Val273Ile)
c.619G>A (p.Val207Ile)
n.889G>A
n.879G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47414293G>CCA346732773MSH2c.817G>C (p.Val273Leu)
c.619G>C (p.Val207Leu)
n.889G>C
n.879G>C
 dbSNP
2g.47414293G=CA2495833904MSH2c.817G= (p.Val273=)
c.619G= (p.Val207=)
n.889G=
n.879G=
2g.47414293G>TCA346732774MSH2c.817G>T (p.Val273Leu)
c.619G>T (p.Val207Leu)
n.889G>T
n.879G>T
 ClinVar dbSNP
2g.47414293_47414294delinsAACA022365MSH2c.817_818delinsAA (p.Val273Lys)
c.619_620delinsAA (p.Val207Lys)
n.889_890delinsAA
n.879_880delinsAA
 dbSNP
2g.47414293_47414294delinsGTCA2495833903MSH2c.817_818delinsGT (p.Val273=)
c.619_620delinsGT (p.Val207=)
n.889_890delinsGT
n.879_880delinsGT
2g.47414294delCA913090558MSH2c.818del (p.Val273GlufsTer5)
c.620del (p.Val207GlufsTer5)
n.890del
n.880del
2g.47414294T>ACA346732775MSH2c.818T>A (p.Val273Glu)
c.620T>A (p.Val207Glu)
n.890T>A
n.880T>A
2g.47414294T>CCA040789MSH2c.818T>C (p.Val273Ala)
c.620T>C (p.Val207Ala)
n.890T>C
n.880T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47414294T>GCA346732776MSH2c.818T>G (p.Val273Gly)
c.620T>G (p.Val207Gly)
n.890T>G
n.880T>G
2g.47414294T=CA2495833913MSH2c.818T= (p.Val273=)
c.620T= (p.Val207=)
n.890T=
n.880T=
2g.47414294_47414297delinsTAATCA2495833916MSH2c.818_821delinsTAAT (p.Val273=)
c.620_623delinsTAAT (p.Val207=)
n.890_893delinsTAAT
n.880_883delinsTAAT
2g.47414295A=CA2495833926MSH2c.819A= (p.Val273=)
c.621A= (p.Val207=)
n.891A=
n.881A=
2g.47414295A>CCA425969734MSH2c.819A>C (p.Val273=)
c.621A>C (p.Val207=)
n.891A>C
n.881A>C
2g.47414295A>GCA022370MSH2c.819A>G (p.Val273=)
c.621A>G (p.Val207=)
n.891A>G
n.881A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47414295A>TCA425969737MSH2c.819A>T (p.Val273=)
c.621A>T (p.Val207=)
n.891A>T
n.881A>T
 dbSNP gnomAD v4
2g.47414295_47414297delinsTGCA349973MSH2c.819_821delinsTG (p.Ile274AlafsTer4)
c.621_623delinsTG (p.Ile208AlafsTer4)
n.891_893delinsTG
n.881_883delinsTG
 ClinVar dbSNP
2g.47414296A=CA2495833935MSH2c.820A= (p.Ile274=)
c.622A= (p.Ile208=)
n.892A=
n.882A=
2g.47414296A>CCA346732777MSH2c.820A>C (p.Ile274Leu)
c.622A>C (p.Ile208Leu)
n.892A>C
n.882A>C
 ClinVar dbSNP
2g.47414296A>GCA022377MSH2c.820A>G (p.Ile274Val)
c.622A>G (p.Ile208Val)
n.892A>G
n.882A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47414296A>TCA346732778MSH2c.820A>T (p.Ile274Phe)
c.622A>T (p.Ile208Phe)
n.892A>T
n.882A>T
 dbSNP
2g.47414297T>ACA346732779MSH2c.821T>A (p.Ile274Asn)
c.623T>A (p.Ile208Asn)
n.893T>A
n.883T>A
 dbSNP gnomAD v4
2g.47414297T>CCA346732780MSH2c.821T>C (p.Ile274Thr)
c.623T>C (p.Ile208Thr)
n.893T>C
n.883T>C
 dbSNP
2g.47414297T>GCA346732781MSH2c.821T>G (p.Ile274Ser)
c.623T>G (p.Ile208Ser)
n.893T>G
n.883T>G
 dbSNP
2g.47414297_47414298insGCA2499216017MSH2c.821_822insG (p.Ile274MetfsTer10)
c.623_624insG (p.Ile208MetfsTer10)
n.893_894insG
n.883_884insG
 dbSNP
2g.47414298C>ACA425969748MSH2c.822C>A (p.Ile274=)
c.624C>A (p.Ile208=)
n.894C>A
n.884C>A
 ClinVar gnomAD v4
2g.47414298C=CA2495833938MSH2c.822C= (p.Ile274=)
c.624C= (p.Ile208=)
n.894C=
n.884C=
2g.47414298C>GCA46683968MSH2c.822C>G (p.Ile274Met)
c.624C>G (p.Ile208Met)
n.894C>G
n.884C>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47414298C>TCA425969749MSH2c.822C>T (p.Ile274=)
c.624C>T (p.Ile208=)
n.894C>T
n.884C>T
 ClinVar dbSNP
2g.47414299A=CA2495833939MSH2c.823A= (p.Lys275=)
c.625A= (p.Lys209=)
n.895A=
n.885A=
2g.47414299A>CCA346732784MSH2c.823A>C (p.Lys275Gln)
c.625A>C (p.Lys209Gln)
n.895A>C
n.885A>C
 ClinVar dbSNP
2g.47414299A>GCA346732782MSH2c.823A>G (p.Lys275Glu)
c.625A>G (p.Lys209Glu)
n.895A>G
n.885A>G
 gnomAD v4
2g.47414299A>TCA346732783MSH2c.823A>T (p.Lys275Ter)
c.625A>T (p.Lys209Ter)
n.895A>T
n.885A>T
 dbSNP
2g.47414300A=CA2495833940MSH2c.824A= (p.Lys275=)
c.626A= (p.Lys209=)
n.896A=
n.886A=
2g.47414300A>CCA346732785MSH2c.824A>C (p.Lys275Thr)
c.626A>C (p.Lys209Thr)
n.896A>C
n.886A>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47414300A>GCA346732786MSH2c.824A>G (p.Lys275Arg)
c.626A>G (p.Lys209Arg)
n.896A>G
n.886A>G
 ClinVar dbSNP gnomAD v4
2g.47414300A>TCA346732787MSH2c.824A>T (p.Lys275Met)
c.626A>T (p.Lys209Met)
n.896A>T
n.886A>T
 dbSNP
2g.47414301G>ACA425969767MSH2c.825G>A (p.Lys275=)
c.627G>A (p.Lys209=)
n.897G>A
n.887G>A
 ClinVar dbSNP gnomAD v4
2g.47414301G>CCA346732788MSH2c.825G>C (p.Lys275Asn)
c.627G>C (p.Lys209Asn)
n.897G>C
n.887G>C
2g.47414301G=CA2495833941MSH2c.825G= (p.Lys275=)
c.627G= (p.Lys209=)
n.897G=
n.887G=
2g.47414301G>TCA346732789MSH2c.825G>T (p.Lys275Asn)
c.627G>T (p.Lys209Asn)
n.897G>T
n.887G>T
2g.47414302T>ACA346732790MSH2c.826T>A (p.Phe276Ile)
c.628T>A (p.Phe210Ile)
n.898T>A
n.888T>A
 ClinVar dbSNP
2g.47414302T>CCA346732792MSH2c.826T>C (p.Phe276Leu)
c.628T>C (p.Phe210Leu)
n.898T>C
n.888T>C
2g.47414302T>GCA346732791MSH2c.826T>G (p.Phe276Val)
c.628T>G (p.Phe210Val)
n.898T>G
n.888T>G
 ClinVar
2g.47414302T=CA2495833942MSH2c.826T= (p.Phe276=)
c.628T= (p.Phe210=)
n.898T=
n.888T=
2g.47414306delCA2499216018MSH2c.830del (p.Leu277Ter)
c.632del (p.Leu211Ter)
n.902del
n.892del
 ClinVar dbSNP
2g.47414303T>ACA346732793MSH2c.827T>A (p.Phe276Tyr)
c.629T>A (p.Phe210Tyr)
n.899T>A
n.889T>A
 dbSNP
2g.47414303T>CCA346732794MSH2c.827T>C (p.Phe276Ser)
c.629T>C (p.Phe210Ser)
n.899T>C
n.889T>C
2g.47414303T>GCA346732795MSH2c.827T>G (p.Phe276Cys)
c.629T>G (p.Phe210Cys)
n.899T>G
n.889T>G
 ClinVar dbSNP
2g.47414304T>ACA346732796MSH2c.828T>A (p.Phe276Leu)
c.630T>A (p.Phe210Leu)
n.900T>A
n.890T>A
2g.47414304T>CCA425969781MSH2c.828T>C (p.Phe276=)
c.630T>C (p.Phe210=)
n.900T>C
n.890T>C
2g.47414304T>GCA346732797MSH2c.828T>G (p.Phe276Leu)
c.630T>G (p.Phe210Leu)
n.900T>G
n.890T>G
2g.47414305T>ACA346732798MSH2c.829T>A (p.Leu277Ile)
c.631T>A (p.Leu211Ile)
n.901T>A
n.891T>A
 dbSNP
2g.47414305T>CCA425969784MSH2c.829T>C (p.Leu277=)
c.631T>C (p.Leu211=)
n.901T>C
n.891T>C
2g.47414305T>GCA346732799MSH2c.829T>G (p.Leu277Val)
c.631T>G (p.Leu211Val)
n.901T>G
n.891T>G
2g.47414306T>ACA16610850MSH2c.830T>A (p.Leu277Ter)
c.632T>A (p.Leu211Ter)
n.902T>A
n.892T>A
 ClinVar dbSNP
2g.47414306T>CCA346732800MSH2c.830T>C (p.Leu277Ser)
c.632T>C (p.Leu211Ser)
n.902T>C
n.892T>C
 ClinVar dbSNP gnomAD v4
2g.47414306T>GCA022392MSH2c.830T>G (p.Leu277Ter)
c.632T>G (p.Leu211Ter)
n.902T>G
n.892T>G
 ClinVar dbSNP
2g.47414306T=CA2495833943MSH2c.830T= (p.Leu277=)
c.632T= (p.Leu211=)
n.902T=
n.892T=
2g.47414306_47414308delinsTAGCA2495833944MSH2c.830_832delinsTAG (p.Leu277=)
c.632_634delinsTAG (p.Leu211=)
n.902_904delinsTAG
n.892_894delinsTAG
2g.47414307A>CCA346732801MSH2c.831A>C (p.Leu277Phe)
c.633A>C (p.Leu211Phe)
n.903A>C
n.893A>C
2g.47414307A>GCA425969793MSH2c.831A>G (p.Leu277=)
c.633A>G (p.Leu211=)
n.903A>G
n.893A>G
 ClinVar dbSNP gnomAD v4
2g.47414307A>TCA346732802MSH2c.831A>T (p.Leu277Phe)
c.633A>T (p.Leu211Phe)
n.903A>T
n.893A>T
 dbSNP
2g.47414308_47414309delCA913187889MSH2c.832_833del (p.Glu278ThrfsTer5)
c.634_635del (p.Glu212ThrfsTer5)
n.904_905del
n.894_895del
 ClinVar dbSNP
2g.47414308delCA2586969212MSH2c.832del (p.Glu278AsnfsTer14)
c.634del (p.Glu212AsnfsTer14)
n.904del
n.894del
2g.47414308G>ACA346732803MSH2c.832G>A (p.Glu278Lys)
c.634G>A (p.Glu212Lys)
n.904G>A
n.894G>A
 ClinVar dbSNP
2g.47414308G>CCA346732805MSH2c.832G>C (p.Glu278Gln)
c.634G>C (p.Glu212Gln)
n.904G>C
n.894G>C
 dbSNP
2g.47414308G=CA2495833945MSH2c.832G= (p.Glu278=)
c.634G= (p.Glu212=)
n.904G=
n.894G=
2g.47414308G>TCA346732804MSH2c.832G>T (p.Glu278Ter)
c.634G>T (p.Glu212Ter)
n.904G>T
n.894G>T
 ClinVar dbSNP
2g.47414309A=CA2495833946MSH2c.833A= (p.Glu278=)
c.635A= (p.Glu212=)
n.905A=
n.895A=
2g.47414309A>CCA346732806MSH2c.833A>C (p.Glu278Ala)
c.635A>C (p.Glu212Ala)
n.905A>C
n.895A>C
 dbSNP
2g.47414309A>GCA346732808MSH2c.833A>G (p.Glu278Gly)
c.635A>G (p.Glu212Gly)
n.905A>G
n.895A>G
 ClinVar dbSNP
2g.47414309A>TCA346732807MSH2c.833A>T (p.Glu278Val)
c.635A>T (p.Glu212Val)
n.905A>T
n.895A>T
 dbSNP
2g.47414310A=CA2495833947MSH2c.834A= (p.Glu278=)
c.636A= (p.Glu212=)
n.906A=
n.896A=
2g.47414310A>CCA346732809MSH2c.834A>C (p.Glu278Asp)
c.636A>C (p.Glu212Asp)
n.906A>C
n.896A>C
2g.47414310A>GCA10577955MSH2c.834A>G (p.Glu278=)
c.636A>G (p.Glu212=)
n.906A>G
n.896A>G
 ClinVar dbSNP
2g.47414310A>TCA346732810MSH2c.834A>T (p.Glu278Asp)
c.636A>T (p.Glu212Asp)
n.906A>T
n.896A>T
 dbSNP
2g.47414310_47414311insTCA2586969213MSH2c.834_835insT (p.Leu279SerfsTer5)
c.636_637insT (p.Leu213SerfsTer5)
n.906_907insT
n.896_897insT
2g.47414311C>ACA346732811MSH2c.835C>A (p.Leu279Ile)
c.637C>A (p.Leu213Ile)
n.907C>A
n.897C>A
 dbSNP
2g.47414311C=CA2495833948MSH2c.835C= (p.Leu279=)
c.637C= (p.Leu213=)
n.907C=
n.897C=
2g.47414311C>GCA022395MSH2c.835C>G (p.Leu279Val)
c.637C>G (p.Leu213Val)
n.907C>G
n.897C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47414311C>TCA46683989MSH2c.835C>T (p.Leu279Phe)
c.637C>T (p.Leu213Phe)
n.907C>T
n.897C>T
 dbSNP
2g.47414311_47414312delinsCTCA2495833950MSH2c.835_836delinsCT (p.Leu279=)
c.637_638delinsCT (p.Leu213=)
n.907_908delinsCT
n.897_898delinsCT
2g.47414311_47414314delinsCTCTCA2495833949MSH2c.835_838delinsCTCT (p.Leu279=)
c.637_640delinsCTCT (p.Leu213=)
n.907_910delinsCTCT
n.897_900delinsCTCT
2g.47414311_47414318dupCA2739274422MSH2c.835_842dup (p.Asp282SerfsTer13)
c.637_644dup (p.Asp216SerfsTer13)
n.907_914dup
n.897_904dup
 ClinVar
2g.47414312delCA022401MSH2c.836del (p.Leu279ProfsTer13)
c.638del (p.Leu213ProfsTer13)
n.908del
n.898del
 ClinVar dbSNP
2g.47414312T>ACA346732812MSH2c.836T>A (p.Leu279His)
c.638T>A (p.Leu213His)
n.908T>A
n.898T>A
 ClinVar dbSNP
2g.47414312T>CCA46683995MSH2c.836T>C (p.Leu279Pro)
c.638T>C (p.Leu213Pro)
n.908T>C
n.898T>C
 ClinVar dbSNP gnomAD v4
2g.47414312T>GCA346732813MSH2c.836T>G (p.Leu279Arg)
c.638T>G (p.Leu213Arg)
n.908T>G
n.898T>G
 ClinVar
2g.47414312T=CA2495833951MSH2c.836T= (p.Leu279=)
c.638T= (p.Leu213=)
n.908T=
n.898T=
2g.47414313_47414315delCA46684001MSH2c.837_839del (p.Leu280del)
c.639_641del (p.Leu214del)
n.909_911del
n.899_901del
 dbSNP
2g.47414313C>ACA425969824MSH2c.837C>A (p.Leu279=)
c.639C>A (p.Leu213=)
n.909C>A
n.899C>A
 dbSNP
2g.47414313C=CA2495833952MSH2c.837C= (p.Leu279=)
c.639C= (p.Leu213=)
n.909C=
n.899C=
2g.47414313C>GCA040865MSH2c.837C>G (p.Leu279=)
c.639C>G (p.Leu213=)
n.909C>G
n.899C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47414313C>TCA16610801MSH2c.837C>T (p.Leu279=)
c.639C>T (p.Leu213=)
n.909C>T
n.899C>T
 ClinVar dbSNP
2g.47414313_47414314delinsCTCA2495833953MSH2c.837_838delinsCT (p.Leu279=)
c.639_640delinsCT (p.Leu213=)
n.909_910delinsCT
n.899_900delinsCT
2g.47414318_47414507delCA2580067008MSH2c.842_942+89del
c.644_744+89del
n.914_1014+89del
n.904_1004+89del
 ClinVar
2g.47414314T>ACA346732814MSH2c.838T>A (p.Leu280Ile)
c.640T>A (p.Leu214Ile)
n.910T>A
n.900T>A
2g.47414314T>CCA425969832MSH2c.838T>C (p.Leu280=)
c.640T>C (p.Leu214=)
n.910T>C
n.900T>C
 ClinVar dbSNP gnomAD v4
2g.47414314T>GCA346732815MSH2c.838T>G (p.Leu280Val)
c.640T>G (p.Leu214Val)
n.910T>G
n.900T>G
2g.47414314T=CA2495833954MSH2c.838T= (p.Leu280=)
c.640T= (p.Leu214=)
n.910T=
n.900T=
2g.47414315dupCA022405MSH2c.839dup (p.Leu280PhefsTer4)
c.641dup (p.Leu214PhefsTer4)
n.911dup
n.901dup
 ClinVar dbSNP
2g.47414315delCA658683221MSH2c.839del (p.Leu280TyrfsTer12)
c.641del (p.Leu214TyrfsTer12)
n.911del
n.901del
 ClinVar dbSNP
2g.47414315T>ACA346732816MSH2c.839T>A (p.Leu280Ter)
c.641T>A (p.Leu214Ter)
n.911T>A
n.901T>A
 ClinVar dbSNP
2g.47414315T>CCA346732817MSH2c.839T>C (p.Leu280Ser)
c.641T>C (p.Leu214Ser)
n.911T>C
n.901T>C
 ClinVar dbSNP
2g.47414315T>GCA346732818MSH2c.839T>G (p.Leu280Ter)
c.641T>G (p.Leu214Ter)
n.911T>G
n.901T>G
 ClinVar
2g.47414315T=CA2495833956MSH2c.839T= (p.Leu280=)
c.641T= (p.Leu214=)
n.911T=
n.901T=
2g.47414315_47414316delinsTACA2495833955MSH2c.839_840delinsTA (p.Leu280=)
c.641_642delinsTA (p.Leu214=)
n.911_912delinsTA
n.901_902delinsTA
2g.47414316delCA46684014MSH2c.840del (p.Leu280PhefsTer12)
c.642del (p.Leu214PhefsTer12)
n.912del
n.902del
 dbSNP
2g.47414316A=CA2495833957MSH2c.840A= (p.Leu280=)
c.642A= (p.Leu214=)
n.912A=
n.902A=
2g.47414316A>CCA346732819MSH2c.840A>C (p.Leu280Phe)
c.642A>C (p.Leu214Phe)
n.912A>C
n.902A>C
 ClinVar dbSNP
2g.47414316A>GCA425969839MSH2c.840A>G (p.Leu280=)
c.642A>G (p.Leu214=)
n.912A>G
n.902A>G
2g.47414316A>TCA346732820MSH2c.840A>T (p.Leu280Phe)
c.642A>T (p.Leu214Phe)
n.912A>T
n.902A>T
 dbSNP
2g.47414316dupCA2580067012MSH2c.840dup (p.Ser281IlefsTer3)
c.642dup (p.Ser215IlefsTer3)
n.912dup
n.902dup
 ClinVar
2g.47414317_47414319delCA2699275827MSH2c.841_843del (p.Ser281del)
c.643_645del (p.Ser215del)
n.913_915del
n.903_905del
 dbSNP
2g.47414317delCA2586969216MSH2c.841del (p.Ser281GlnfsTer11)
c.643del (p.Ser215GlnfsTer11)
n.913del
n.903del
2g.47414317T>ACA346732821MSH2c.841T>A (p.Ser281Thr)
c.643T>A (p.Ser215Thr)
n.913T>A
n.903T>A
 ClinVar dbSNP gnomAD v4
2g.47414317T>CCA022412MSH2c.841T>C (p.Ser281Pro)
c.643T>C (p.Ser215Pro)
n.913T>C
n.903T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47414317T>GCA346732822MSH2c.841T>G (p.Ser281Ala)
c.643T>G (p.Ser215Ala)
n.913T>G
n.903T>G
2g.47414317T=CA2495833958MSH2c.841T= (p.Ser281=)
c.643T= (p.Ser215=)
n.913T=
n.903T=
2g.47414317dupCA2586969215MSH2c.841dup (p.Ser281PhefsTer3)
c.643dup (p.Ser215PhefsTer3)
n.913dup
n.903dup
2g.47414318C>ACA022416MSH2c.842C>A (p.Ser281Ter)
c.644C>A (p.Ser215Ter)
n.914C>A
n.904C>A
 ClinVar dbSNP
2g.47414318C=CA2495833959MSH2c.842C= (p.Ser281=)
c.644C= (p.Ser215=)
n.914C=
n.904C=
2g.47414318C>GCA349474MSH2c.842C>G (p.Ser281Ter)
c.644C>G (p.Ser215Ter)
n.914C>G
n.904C>G
 ClinVar dbSNP
2g.47414318C>TCA346732823MSH2c.842C>T (p.Ser281Leu)
c.644C>T (p.Ser215Leu)
n.914C>T
n.904C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47414319A=CA2495833960MSH2c.843A= (p.Ser281=)
c.645A= (p.Ser215=)
n.915A=
n.905A=
2g.47414319A>CCA425969851MSH2c.843A>C (p.Ser281=)
c.645A>C (p.Ser215=)
n.915A>C
n.905A>C
2g.47414319A>GCA16610774MSH2c.843A>G (p.Ser281=)
c.645A>G (p.Ser215=)
n.915A>G
n.905A>G
 ClinVar dbSNP gnomAD v4
2g.47414319A>TCA040882MSH2c.843A>T (p.Ser281=)
c.645A>T (p.Ser215=)
n.915A>T
n.905A>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47414319_47414320insTCA2580067017MSH2c.843_844insT (p.Asp282Ter)
c.645_646insT (p.Asp216Ter)
n.915_916insT
n.905_906insT
 ClinVar
2g.47414320G>ACA346732824MSH2c.844G>A (p.Asp282Asn)
c.646G>A (p.Asp216Asn)
n.916G>A
n.906G>A
 dbSNP
2g.47414320G>CCA040894MSH2c.844G>C (p.Asp282His)
c.646G>C (p.Asp216His)
n.916G>C
n.906G>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47414320G=CA2495833962MSH2c.844G= (p.Asp282=)
c.646G= (p.Asp216=)
n.916G=
n.906G=
2g.47414320G>TCA346732825MSH2c.844G>T (p.Asp282Tyr)
c.646G>T (p.Asp216Tyr)
n.916G>T
n.906G>T
 dbSNP COSMIC
2g.47414320_47414324delinsGATGACA2495833961MSH2c.844_848delinsGATGA (p.Asp282=)
c.646_650delinsGATGA (p.Asp216=)
n.916_920delinsGATGA
n.906_910delinsGATGA
2g.47414321A=CA2495833963MSH2c.845A= (p.Asp282=)
c.647A= (p.Asp216=)
n.917A=
n.907A=
2g.47414321A>CCA346732826MSH2c.845A>C (p.Asp282Ala)
c.647A>C (p.Asp216Ala)
n.917A>C
n.907A>C
 ClinVar dbSNP
2g.47414321A>GCA022423MSH2c.845A>G (p.Asp282Gly)
c.647A>G (p.Asp216Gly)
n.917A>G
n.907A>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47414321A>TCA346732827MSH2c.845A>T (p.Asp282Val)
c.647A>T (p.Asp216Val)
n.917A>T
n.907A>T
 dbSNP
2g.47414321_47414324delCA658683222MSH2c.845_848del (p.Asp282ValfsTer9)
c.647_650del (p.Asp216ValfsTer9)
n.917_920del
n.907_910del
 ClinVar dbSNP
2g.47414322delCA2697548098MSH2c.846del (p.Asp282GlufsTer10)
c.648del (p.Asp216GlufsTer10)
n.918del
n.908del
 ClinVar
2g.47414322T>ACA346732828MSH2c.846T>A (p.Asp282Glu)
c.648T>A (p.Asp216Glu)
n.918T>A
n.908T>A
 dbSNP
2g.47414322T>CCA425969872MSH2c.846T>C (p.Asp282=)
c.648T>C (p.Asp216=)
n.918T>C
n.908T>C
 ClinVar
2g.47414322T>GCA346732829MSH2c.846T>G (p.Asp282Glu)
c.648T>G (p.Asp216Glu)
n.918T>G
n.908T>G
 ClinVar dbSNP gnomAD v4
2g.47414322T=CA2495833964MSH2c.846T= (p.Asp282=)
c.648T= (p.Asp216=)
n.918T=
n.908T=
2g.47414323delCA2586969217MSH2c.847del (p.Asp283IlefsTer9)
c.649del (p.Asp217IlefsTer9)
n.919del
n.909del
2g.47414323G>ACA346732831MSH2c.847G>A (p.Asp283Asn)
c.649G>A (p.Asp217Asn)
n.919G>A
n.909G>A
 ClinVar dbSNP
2g.47414323G>CCA346732830MSH2c.847G>C (p.Asp283His)
c.649G>C (p.Asp217His)
n.919G>C
n.909G>C
 ClinVar dbSNP
2g.47414323G=CA2495833965MSH2c.847G= (p.Asp283=)
c.649G= (p.Asp217=)
n.919G=
n.909G=
2g.47414323G>TCA022428MSH2c.847G>T (p.Asp283Tyr)
c.649G>T (p.Asp217Tyr)
n.919G>T
n.909G>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47414324A=CA2495833966MSH2c.848A= (p.Asp283=)
c.650A= (p.Asp217=)
n.920A=
n.910A=
2g.47414324A>CCA346732832MSH2c.848A>C (p.Asp283Ala)
c.650A>C (p.Asp217Ala)
n.920A>C
n.910A>C
2g.47414324A>GCA346732833MSH2c.848A>G (p.Asp283Gly)
c.650A>G (p.Asp217Gly)
n.920A>G
n.910A>G
 ClinVar dbSNP
2g.47414324A>TCA040911MSH2c.848A>T (p.Asp283Val)
c.650A>T (p.Asp217Val)
n.920A>T
n.910A>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47414325T>ACA346732834MSH2c.849T>A (p.Asp283Glu)
c.651T>A (p.Asp217Glu)
n.921T>A
n.911T>A
 dbSNP
2g.47414325T>CCA10577956MSH2c.849T>C (p.Asp283=)
c.651T>C (p.Asp217=)
n.921T>C
n.911T>C
 ClinVar dbSNP
2g.47414325T>GCA346732835MSH2c.849T>G (p.Asp283Glu)
c.651T>G (p.Asp217Glu)
n.921T>G
n.911T>G
2g.47414325T=CA2495833967MSH2c.849T= (p.Asp283=)
c.651T= (p.Asp217=)
n.921T=
n.911T=
2g.47414326dupCA645369200MSH2c.850dup (p.Ser284PhefsTer7)
c.652dup (p.Ser218PhefsTer7)
n.922dup
n.912dup
 ClinVar dbSNP
2g.47414326delCA2697548099MSH2c.850del (p.Ser284ProfsTer8)
c.652del (p.Ser218ProfsTer8)
n.922del
n.912del
 ClinVar
2g.47414326T>ACA346732836MSH2c.850T>A (p.Ser284Thr)
c.652T>A (p.Ser218Thr)
n.922T>A
n.912T>A
2g.47414326T>CCA346732838MSH2c.850T>C (p.Ser284Pro)
c.652T>C (p.Ser218Pro)
n.922T>C
n.912T>C
2g.47414326T>GCA346732837MSH2c.850T>G (p.Ser284Ala)
c.652T>G (p.Ser218Ala)
n.922T>G
n.912T>G
2g.47414327C>ACA040934MSH2c.851C>A (p.Ser284Tyr)
c.653C>A (p.Ser218Tyr)
n.923C>A
n.913C>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47414327C=CA2495833968MSH2c.851C= (p.Ser284=)
c.653C= (p.Ser218=)
n.923C=
n.913C=
2g.47414327C>GCA346732839MSH2c.851C>G (p.Ser284Cys)
c.653C>G (p.Ser218Cys)
n.923C>G
n.913C>G
 dbSNP
2g.47414327C>TCA346732840MSH2c.851C>T (p.Ser284Phe)
c.653C>T (p.Ser218Phe)
n.923C>T
n.913C>T
 ClinVar dbSNP
2g.47414328C>ACA425969904MSH2c.852C>A (p.Ser284=)
c.654C>A (p.Ser218=)
n.924C>A
n.914C>A
 dbSNP
2g.47414328C=CA2495833970MSH2c.852C= (p.Ser284=)
c.654C= (p.Ser218=)
n.924C=
n.914C=
2g.47414328C>GCA425969907MSH2c.852C>G (p.Ser284=)
c.654C>G (p.Ser218=)
n.924C>G
n.914C>G
 dbSNP
2g.47414328C>TCA425969903MSH2c.852C>T (p.Ser284=)
c.654C>T (p.Ser218=)
n.924C>T
n.914C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47414328_47414329delinsCACA2495833969MSH2c.852_853delinsCA (p.Ser284=)
c.654_655delinsCA (p.Ser218=)
n.924_925delinsCA
n.914_915delinsCA
2g.47414329A>CCA346732841MSH2c.853A>C (p.Asn285His)
c.655A>C (p.Asn219His)
n.925A>C
n.915A>C
2g.47414329A>GCA346732842MSH2c.853A>G (p.Asn285Asp)
c.655A>G (p.Asn219Asp)
n.925A>G
n.915A>G
2g.47414329A>TCA346732843MSH2c.853A>T (p.Asn285Tyr)
c.655A>T (p.Asn219Tyr)
n.925A>T
n.915A>T
 dbSNP
2g.47414330delCA022433MSH2c.854del (p.Asn285ThrfsTer7)
c.656del (p.Asn219ThrfsTer7)
n.926del
n.916del
 ClinVar dbSNP
2g.47414330A=CA2495833971MSH2c.854A= (p.Asn285=)
c.656A= (p.Asn219=)
n.926A=
n.916A=
2g.47414330A>CCA346732844MSH2c.854A>C (p.Asn285Thr)
c.656A>C (p.Asn219Thr)
n.926A>C
n.916A>C
 ClinVar dbSNP
2g.47414330A>GCA16611014MSH2c.854A>G (p.Asn285Ser)
c.656A>G (p.Asn219Ser)
n.926A>G
n.916A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47414330A>TCA346732845MSH2c.854A>T (p.Asn285Ile)
c.656A>T (p.Asn219Ile)
n.926A>T
n.916A>T
 dbSNP
2g.47414331C>ACA346732846MSH2c.855C>A (p.Asn285Lys)
c.657C>A (p.Asn219Lys)
n.927C>A
n.917C>A
 dbSNP
2g.47414331C=CA2495833974MSH2c.855C= (p.Asn285=)
c.657C= (p.Asn219=)
n.927C=
n.917C=
2g.47414331C>GCA10577957MSH2c.855C>G (p.Asn285Lys)
c.657C>G (p.Asn219Lys)
n.927C>G
n.917C>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47414331C>TCA040947MSH2c.855C>T (p.Asn285=)
c.657C>T (p.Asn219=)
n.927C>T
n.917C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.47414331_47414332delinsCTCA2495833972MSH2c.855_856delinsCT (p.Asn285=)
c.657_658delinsCT (p.Asn219=)
n.927_928delinsCT
n.917_918delinsCT
2g.47414331_47414340delinsCTTTGGACAGCA2495833973MSH2c.855_864delinsCTTTGGACAG (p.Asn285=)
c.657_666delinsCTTTGGACAG (p.Asn219=)
n.927_936delinsCTTTGGACAG
n.917_926delinsCTTTGGACAG
2g.47414332T>ACA346732847MSH2c.856T>A (p.Phe286Ile)
c.658T>A (p.Phe220Ile)
n.928T>A
n.918T>A
2g.47414332T>CCA346732848MSH2c.856T>C (p.Phe286Leu)
c.658T>C (p.Phe220Leu)
n.928T>C
n.918T>C
 dbSNP
2g.47414332T>GCA346732849MSH2c.856T>G (p.Phe286Val)
c.658T>G (p.Phe220Val)
n.928T>G
n.918T>G
2g.47414334delCA658683223MSH2c.858del (p.Phe286LeufsTer6)
c.660del (p.Phe220LeufsTer6)
n.930del
n.920del
 ClinVar dbSNP
2g.47414333_47414334delCA2580067027MSH2c.857_858del (p.Phe286TrpfsTer4)
c.659_660del (p.Phe220TrpfsTer4)
n.929_930del
n.919_920del
 ClinVar
2g.47414336_47414344delCA349908MSH2c.860_868del (p.Gly287_Phe289del)
c.662_670del (p.Gly221_Phe223del)
n.932_940del
n.922_930del
 dbSNP
2g.47414333T>ACA346732850MSH2c.857T>A (p.Phe286Tyr)
c.659T>A (p.Phe220Tyr)
n.929T>A
n.919T>A
 dbSNP
2g.47414333T>CCA346732851MSH2c.857T>C (p.Phe286Ser)
c.659T>C (p.Phe220Ser)
n.929T>C
n.919T>C
 ClinVar dbSNP
2g.47414333T>GCA346732852MSH2c.857T>G (p.Phe286Cys)
c.659T>G (p.Phe220Cys)
n.929T>G
n.919T>G
2g.47414333T=CA2495833975MSH2c.857T= (p.Phe286=)
c.659T= (p.Phe220=)
n.929T=
n.919T=
2g.47414334T>ACA346732853MSH2c.858T>A (p.Phe286Leu)
c.660T>A (p.Phe220Leu)
n.930T>A
n.920T>A
2g.47414334T>CCA425969946MSH2c.858T>C (p.Phe286=)
c.660T>C (p.Phe220=)
n.930T>C
n.920T>C
 ClinVar dbSNP gnomAD v4
2g.47414334T>GCA346732854MSH2c.858T>G (p.Phe286Leu)
c.660T>G (p.Phe220Leu)
n.930T>G
n.920T>G
2g.47414334T=CA2495833976MSH2c.858T= (p.Phe286=)
c.660T= (p.Phe220=)
n.930T=
n.920T=
2g.47414335G>ACA346732856MSH2c.859G>A (p.Gly287Arg)
c.661G>A (p.Gly221Arg)
n.931G>A
n.921G>A
 ClinVar dbSNP
2g.47414335G>CCA346732855MSH2c.859G>C (p.Gly287Arg)
c.661G>C (p.Gly221Arg)
n.931G>C
n.921G>C
 ClinVar dbSNP
2g.47414335G=CA2495833977MSH2c.859G= (p.Gly287=)
c.661G= (p.Gly221=)
n.931G=
n.921G=
2g.47414335G>TCA022437MSH2c.859G>T (p.Gly287Ter)
c.661G>T (p.Gly221Ter)
n.931G>T
n.921G>T
 ClinVar dbSNP
2g.47414336dupCA186235MSH2c.860dup (p.Gln288ThrfsTer3)
c.662dup (p.Gln222ThrfsTer3)
n.932dup
n.922dup
 ClinVar dbSNP
2g.47414336G>ACA346732857MSH2c.860G>A (p.Gly287Glu)
c.662G>A (p.Gly221Glu)
n.932G>A
n.922G>A
 ClinVar dbSNP gnomAD v4
2g.47414336G>CCA022444MSH2c.860G>C (p.Gly287Ala)
c.662G>C (p.Gly221Ala)
n.932G>C
n.922G>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47414336G=CA2495833978MSH2c.860G= (p.Gly287=)
c.662G= (p.Gly221=)
n.932G=
n.922G=
2g.47414336G>TCA346732858MSH2c.860G>T (p.Gly287Val)
c.662G>T (p.Gly221Val)
n.932G>T
n.922G>T
 dbSNP gnomAD v4
2g.47414337A>CCA425969965MSH2c.861A>C (p.Gly287=)
c.663A>C (p.Gly221=)
n.933A>C
n.923A>C
 dbSNP
2g.47414337A>GCA425969963MSH2c.861A>G (p.Gly287=)
c.663A>G (p.Gly221=)
n.933A>G
n.923A>G
 ClinVar gnomAD v4
2g.47414337A>TCA425969962MSH2c.861A>T (p.Gly287=)
c.663A>T (p.Gly221=)
n.933A>T
n.923A>T
 dbSNP
2g.47414338C>ACA346732859MSH2c.862C>A (p.Gln288Lys)
c.664C>A (p.Gln222Lys)
n.934C>A
n.924C>A
 dbSNP
2g.47414338C=CA2495833979MSH2c.862C= (p.Gln288=)
c.664C= (p.Gln222=)
n.934C=
n.924C=
2g.47414338C>GCA346732860MSH2c.862C>G (p.Gln288Glu)
c.664C>G (p.Gln222Glu)
n.934C>G
n.924C>G
 ClinVar dbSNP
2g.47414338C>TCA022450MSH2c.862C>T (p.Gln288Ter)
c.664C>T (p.Gln222Ter)
n.934C>T
n.924C>T
 ClinVar dbSNP
2g.47414338_47414339delinsCACA2495833980MSH2c.862_863delinsCA (p.Gln288=)
c.664_665delinsCA (p.Gln222=)
n.934_935delinsCA
n.924_925delinsCA
2g.47414339delCA022453MSH2c.863del (p.Gln288ArgfsTer4)
c.665del (p.Gln222ArgfsTer4)
n.935del
n.925del
 ClinVar dbSNP
2g.47414339A=CA2495833981MSH2c.863A= (p.Gln288=)
c.665A= (p.Gln222=)
n.935A=
n.925A=
2g.47414339A>CCA346732861MSH2c.863A>C (p.Gln288Pro)
c.665A>C (p.Gln222Pro)
n.935A>C
n.925A>C
2g.47414339A>GCA346732862MSH2c.863A>G (p.Gln288Arg)
c.665A>G (p.Gln222Arg)
n.935A>G
n.925A>G
 ClinVar dbSNP gnomAD v2
2g.47414339A>TCA346732863MSH2c.863A>T (p.Gln288Leu)
c.665A>T (p.Gln222Leu)
n.935A>T
n.925A>T
 dbSNP
2g.47414340G>ACA425969980MSH2c.864G>A (p.Gln288=)
c.666G>A (p.Gln222=)
n.936G>A
n.926G>A
 ClinVar dbSNP gnomAD v4
2g.47414340G>CCA346732864MSH2c.864G>C (p.Gln288His)
c.666G>C (p.Gln222His)
n.936G>C
n.926G>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47414340G=CA2495833982MSH2c.864G= (p.Gln288=)
c.666G= (p.Gln222=)
n.936G=
n.926G=
2g.47414340G>TCA346732865MSH2c.864G>T (p.Gln288His)
c.666G>T (p.Gln222His)
n.936G>T
n.926G>T
2g.47414340_47414341delinsGTCA2495833983MSH2c.864_865delinsGT (p.Gln288=)
c.666_667delinsGT (p.Gln222=)
n.936_937delinsGT
n.926_927delinsGT
2g.47414341T>ACA346732866MSH2c.865T>A (p.Phe289Ile)
c.667T>A (p.Phe223Ile)
n.937T>A
n.927T>A
 dbSNP
2g.47414341T>CCA16611016MSH2c.865T>C (p.Phe289Leu)
c.667T>C (p.Phe223Leu)
n.937T>C
n.927T>C
 ClinVar dbSNP
2g.47414341T>GCA346732867MSH2c.865T>G (p.Phe289Val)
c.667T>G (p.Phe223Val)
n.937T>G
n.927T>G
2g.47414341T=CA2495833984MSH2c.865T= (p.Phe289=)
c.667T= (p.Phe223=)
n.937T=
n.927T=
2g.47414343dupCA2580067034MSH2c.867dup (p.Glu290Ter)
c.669dup (p.Glu224Ter)
n.939dup
n.929dup
 ClinVar
2g.47414342_47414343dupCA1139656933MSH2c.866_867dup (p.Glu290LeufsTer3)
c.668_669dup (p.Glu224LeufsTer3)
n.938_939dup
n.928_929dup
 ClinVar dbSNP
2g.47414343delCA916080253MSH2c.867del (p.Phe289LeufsTer3)
c.669del (p.Phe223LeufsTer3)
n.939del
n.929del
 ClinVar dbSNP
2g.47414342T>ACA346732868MSH2c.866T>A (p.Phe289Tyr)
c.668T>A (p.Phe223Tyr)
n.938T>A
n.928T>A
2g.47414342T>CCA346732869MSH2c.866T>C (p.Phe289Ser)
c.668T>C (p.Phe223Ser)
n.938T>C
n.928T>C
2g.47414342T>GCA346732870MSH2c.866T>G (p.Phe289Cys)
c.668T>G (p.Phe223Cys)
n.938T>G
n.928T>G
2g.47414342_47414347delinsTTGAACCA2495833985MSH2c.866_871delinsTTGAAC (p.Phe289=)
c.668_673delinsTTGAAC (p.Phe223=)
n.938_943delinsTTGAAC
n.928_933delinsTTGAAC
2g.47414343T>ACA346732872MSH2c.867T>A (p.Phe289Leu)
c.669T>A (p.Phe223Leu)
n.939T>A
n.929T>A
2g.47414343T>CCA337775MSH2c.867T>C (p.Phe289=)
c.669T>C (p.Phe223=)
n.939T>C
n.929T>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47414343T>GCA346732871MSH2c.867T>G (p.Phe289Leu)
c.669T>G (p.Phe223Leu)
n.939T>G
n.929T>G
2g.47414343T=CA2495833986MSH2c.867T= (p.Phe289=)
c.669T= (p.Phe223=)
n.939T=
n.929T=
2g.47414346_47414350delCA645369207MSH2c.870_874del (p.Glu290AspfsTer4)
c.672_676del (p.Glu224AspfsTer4)
n.942_946del
n.932_936del
 ClinVar dbSNP
2g.47414344G>ACA346732873MSH2c.868G>A (p.Glu290Lys)
c.670G>A (p.Glu224Lys)
n.940G>A
n.930G>A
 dbSNP
2g.47414344G>CCA346732874MSH2c.868G>C (p.Glu290Gln)
c.670G>C (p.Glu224Gln)
n.940G>C
n.930G>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47414344G=CA2495833987MSH2c.868G= (p.Glu290=)
c.670G= (p.Glu224=)
n.940G=
n.930G=
2g.47414344G>TCA022458MSH2c.868G>T (p.Glu290Ter)
c.670G>T (p.Glu224Ter)
n.940G>T
n.930G>T
 ClinVar dbSNP
2g.47414344_47414345delCA2580067039MSH2c.868_869del (p.Glu290ThrfsTer5)
c.670_671del (p.Glu224ThrfsTer5)
n.940_941del
n.930_931del
 ClinVar
2g.47414345A>CCA346732875MSH2c.869A>C (p.Glu290Ala)
c.671A>C (p.Glu224Ala)
n.941A>C
n.931A>C
2g.47414345A>GCA346732876MSH2c.869A>G (p.Glu290Gly)
c.671A>G (p.Glu224Gly)
n.941A>G
n.931A>G
 ClinVar gnomAD v4
2g.47414345A>TCA346732877MSH2c.869A>T (p.Glu290Val)
c.671A>T (p.Glu224Val)
n.941A>T
n.931A>T
 dbSNP
2g.47414346delCA2586969219MSH2c.870del (p.Glu290AspfsTer2)
c.672del (p.Glu224AspfsTer2)
n.942del
n.932del
2g.47414345_47414349delinsAACTGCA2495833988MSH2c.869_873delinsAACTG (p.Glu290=)
c.671_675delinsAACTG (p.Glu224=)
n.941_945delinsAACTG
n.931_935delinsAACTG
2g.47414346A>CCA346732879MSH2c.870A>C (p.Glu290Asp)
c.672A>C (p.Glu224Asp)
n.942A>C
n.932A>C
2g.47414346A>GCA425970011MSH2c.870A>G (p.Glu290=)
c.672A>G (p.Glu224=)
n.942A>G
n.932A>G
 ClinVar dbSNP gnomAD v4
2g.47414346A>TCA346732878MSH2c.870A>T (p.Glu290Asp)
c.672A>T (p.Glu224Asp)
n.942A>T
n.932A>T
 ClinVar dbSNP
2g.47414346_47414347delinsACCA2495833989MSH2c.870_871delinsAC (p.Glu290=)
c.672_673delinsAC (p.Glu224=)
n.942_943delinsAC
n.932_933delinsAC
2g.47414349_47414352delCA022463MSH2c.873_876del (p.Thr292LeufsTer8)
c.675_678del (p.Thr226LeufsTer8)
n.945_948del
n.935_938del
 ClinVar dbSNP
2g.47414347delCA16617566MSH2c.871del (p.Leu291Ter)
c.673del (p.Leu225Ter)
n.943del
n.933del
 ClinVar dbSNP
2g.47414347C>ACA346732880MSH2c.871C>A (p.Leu291Met)
c.673C>A (p.Leu225Met)
n.943C>A
n.933C>A
 dbSNP
2g.47414347C=CA2495833990MSH2c.871C= (p.Leu291=)
c.673C= (p.Leu225=)
n.943C=
n.933C=
2g.47414347C>GCA10582005MSH2c.871C>G (p.Leu291Val)
c.673C>G (p.Leu225Val)
n.943C>G
n.933C>G
 ClinVar dbSNP
2g.47414347C>TCA425970021MSH2c.871C>T (p.Leu291=)
c.673C>T (p.Leu225=)
n.943C>T
n.933C>T
 dbSNP
2g.47414347_47414348dupCA2695200780MSH2c.871_872dup (p.Thr292Ter)
c.673_674dup (p.Thr226Ter)
n.943_944dup
n.933_934dup
 ClinVar
2g.47414348T>ACA346732881MSH2c.872T>A (p.Leu291Gln)
c.674T>A (p.Leu225Gln)
n.944T>A
n.934T>A
2g.47414348T>CCA346732882MSH2c.872T>C (p.Leu291Pro)
c.674T>C (p.Leu225Pro)
n.944T>C
n.934T>C
2g.47414348T>GCA346732883MSH2c.872T>G (p.Leu291Arg)
c.674T>G (p.Leu225Arg)
n.944T>G
n.934T>G
2g.47414349delCA2580067041MSH2c.873del (p.Thr292LeufsTer9)
c.675del (p.Thr226LeufsTer9)
n.945del
n.935del
 ClinVar
2g.47414349G>ACA425970026MSH2c.873G>A (p.Leu291=)
c.675G>A (p.Leu225=)
n.945G>A
n.935G>A
 ClinVar dbSNP gnomAD v4
2g.47414349G>CCA425970028MSH2c.873G>C (p.Leu291=)
c.675G>C (p.Leu225=)
n.945G>C
n.935G>C
 dbSNP
2g.47414349G>TCA425970030MSH2c.873G>T (p.Leu291=)
c.675G>T (p.Leu225=)
n.945G>T
n.935G>T
 dbSNP
2g.47414349_47414351delinsGACCA2495833991MSH2c.873_875delinsGAC (p.Leu291=)
c.675_677delinsGAC (p.Leu225=)
n.945_947delinsGAC
n.935_937delinsGAC
2g.47414350A=CA2495833992MSH2c.874A= (p.Thr292=)
c.676A= (p.Thr226=)
n.946A=
n.936A=
2g.47414350A>CCA346732885MSH2c.874A>C (p.Thr292Pro)
c.676A>C (p.Thr226Pro)
n.946A>C
n.936A>C
 ClinVar dbSNP
2g.47414350A>GCA346732884MSH2c.874A>G (p.Thr292Ala)
c.676A>G (p.Thr226Ala)
n.946A>G
n.936A>G
 ClinVar dbSNP
2g.47414350A>TCA022468MSH2c.874A>T (p.Thr292Ser)
c.676A>T (p.Thr226Ser)
n.946A>T
n.936A>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47414350_47414351delCA915943891MSH2c.874_875del (p.Thr292TyrfsTer3)
c.676_677del (p.Thr226TyrfsTer3)
n.946_947del
n.936_937del
 ClinVar dbSNP
2g.47414351C>ACA346732886MSH2c.875C>A (p.Thr292Asn)
c.677C>A (p.Thr226Asn)
n.947C>A
n.937C>A
 dbSNP
2g.47414351C=CA2495833993MSH2c.875C= (p.Thr292=)
c.677C= (p.Thr226=)
n.947C=
n.937C=
2g.47414351C>GCA346732887MSH2c.875C>G (p.Thr292Ser)
c.677C>G (p.Thr226Ser)
n.947C>G
n.937C>G
 dbSNP
2g.47414351C>TCA346732888MSH2c.875C>T (p.Thr292Ile)
c.677C>T (p.Thr226Ile)
n.947C>T
n.937C>T
 ClinVar dbSNP
2g.47414352T>ACA425970043MSH2c.876T>A (p.Thr292=)
c.678T>A (p.Thr226=)
n.948T>A
n.938T>A
 dbSNP
2g.47414352T>CCA425970044MSH2c.876T>C (p.Thr292=)
c.678T>C (p.Thr226=)
n.948T>C
n.938T>C
 ClinVar dbSNP gnomAD v4
2g.47414352T>GCA425970047MSH2c.876T>G (p.Thr292=)
c.678T>G (p.Thr226=)
n.948T>G
n.938T>G
 dbSNP
2g.47414352T=CA2495833994MSH2c.876T= (p.Thr292=)
c.678T= (p.Thr226=)
n.948T=
n.938T=
2g.47414352dupCA16617567MSH2c.876dup (p.Thr293TyrfsTer3)
c.678dup (p.Thr227TyrfsTer3)
n.948dup
n.938dup
 ClinVar dbSNP
2g.47414352_47414353insCCA658760379MSH2c.876_877insC (p.Thr293HisfsTer3)
c.678_679insC (p.Thr227HisfsTer3)
n.948_949insC
n.938_939insC
2g.47414353A=CA2495833995MSH2c.877A= (p.Thr293=)
c.679A= (p.Thr227=)
n.949A=
n.939A=
2g.47414353A>CCA346732889MSH2c.877A>C (p.Thr293Pro)
c.679A>C (p.Thr227Pro)
n.949A>C
n.939A>C
 dbSNP gnomAD v4
2g.47414353A>GCA346732890MSH2c.877A>G (p.Thr293Ala)
c.679A>G (p.Thr227Ala)
n.949A>G
n.939A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47414353A>TCA346732891MSH2c.877A>T (p.Thr293Ser)
c.679A>T (p.Thr227Ser)
n.949A>T
n.939A>T
 dbSNP
2g.47414354C>ACA346732892MSH2c.878C>A (p.Thr293Asn)
c.680C>A (p.Thr227Asn)
n.950C>A
n.940C>A
2g.47414354C=CA2495833997MSH2c.878C= (p.Thr293=)
c.680C= (p.Thr227=)
n.950C=
n.940C=
2g.47414354C>GCA346732893MSH2c.878C>G (p.Thr293Ser)
c.680C>G (p.Thr227Ser)
n.950C>G
n.940C>G
2g.47414354C>TCA346732894MSH2c.878C>T (p.Thr293Ile)
c.680C>T (p.Thr227Ile)
n.950C>T
n.940C>T
 ClinVar dbSNP gnomAD v4
2g.47414354_47414356delinsCTTCA2495833996MSH2c.878_880delinsCTT (p.Thr293=)
c.680_682delinsCTT (p.Thr227=)
n.950_952delinsCTT
n.940_942delinsCTT
2g.47414355T>ACA425970057MSH2c.879T>A (p.Thr293=)
c.681T>A (p.Thr227=)
n.951T>A
n.941T>A
2g.47414355T>CCA425970059MSH2c.879T>C (p.Thr293=)
c.681T>C (p.Thr227=)
n.951T>C
n.941T>C
 dbSNP
2g.47414355T>GCA425970061MSH2c.879T>G (p.Thr293=)
c.681T>G (p.Thr227=)
n.951T>G
n.941T>G
2g.47414355delinsGTACA2580067047MSH2c.879delinsGTA (p.Phe294TyrfsTer8)
c.681delinsGTA (p.Phe228TyrfsTer8)
n.951delinsGTA
n.941delinsGTA
 ClinVar
2g.47414358dupCA2586969222MSH2c.882dup (p.Asp295Ter)
c.684dup (p.Asp229Ter)
n.954dup
n.944dup
2g.47414358delCA913187894MSH2c.882del (p.Phe294LeufsTer7)
c.684del (p.Phe228LeufsTer7)
n.954del
n.944del
 ClinVar dbSNP
2g.47414357_47414358delCA022473MSH2c.881_882del (p.Phe294Ter)
c.683_684del (p.Phe228Ter)
n.953_954del
n.943_944del
 ClinVar dbSNP
2g.47414356_47414363dupCA2499216026MSH2c.880_887dup (p.Ser297LeufsTer7)
c.682_689dup (p.Ser231LeufsTer7)
n.952_959dup
n.942_949dup
 ClinVar dbSNP
2g.47414356T>ACA346732895MSH2c.880T>A (p.Phe294Ile)
c.682T>A (p.Phe228Ile)
n.952T>A
n.942T>A
2g.47414356T>CCA346732896MSH2c.880T>C (p.Phe294Leu)
c.682T>C (p.Phe228Leu)
n.952T>C
n.942T>C
 dbSNP
2g.47414356T>GCA346732897MSH2c.880T>G (p.Phe294Val)
c.682T>G (p.Phe228Val)
n.952T>G
n.942T>G
2g.47414356_47414357insACA2695200781MSH2c.880_881insA (p.Phe294TyrfsTer2)
c.682_683insA (p.Phe228TyrfsTer2)
n.952_953insA
n.942_943insA
 ClinVar
2g.47414357T>ACA346732900MSH2c.881T>A (p.Phe294Tyr)
c.683T>A (p.Phe228Tyr)
n.953T>A
n.943T>A
2g.47414357T>CCA346732898MSH2c.881T>C (p.Phe294Ser)
c.683T>C (p.Phe228Ser)
n.953T>C
n.943T>C
 ClinVar dbSNP
2g.47414357T>GCA346732899MSH2c.881T>G (p.Phe294Cys)
c.683T>G (p.Phe228Cys)
n.953T>G
n.943T>G
 ClinVar dbSNP gnomAD v4
2g.47414357T=CA2495833998MSH2c.881T= (p.Phe294=)
c.683T= (p.Phe228=)
n.953T=
n.943T=
2g.47414358T>ACA346732902MSH2c.882T>A (p.Phe294Leu)
c.684T>A (p.Phe228Leu)
n.954T>A
n.944T>A
 dbSNP
2g.47414358T>CCA425970074MSH2c.882T>C (p.Phe294=)
c.684T>C (p.Phe228=)
n.954T>C
n.944T>C
 dbSNP
2g.47414358T>GCA346732901MSH2c.882T>G (p.Phe294Leu)
c.684T>G (p.Phe228Leu)
n.954T>G
n.944T>G
2g.47414358T=CA2495833999MSH2c.882T= (p.Phe294=)
c.684T= (p.Phe228=)
n.954T=
n.944T=
2g.47414359G>ACA346732905MSH2c.883G>A (p.Asp295Asn)
c.685G>A (p.Asp229Asn)
n.955G>A
n.945G>A
 dbSNP
2g.47414359G>CCA346732903MSH2c.883G>C (p.Asp295His)
c.685G>C (p.Asp229His)
n.955G>C
n.945G>C
 dbSNP
2g.47414359G>TCA346732904MSH2c.883G>T (p.Asp295Tyr)
c.685G>T (p.Asp229Tyr)
n.955G>T
n.945G>T
 ClinVar dbSNP
2g.47414360A>CCA346732906MSH2c.884A>C (p.Asp295Ala)
c.686A>C (p.Asp229Ala)
n.956A>C
n.946A>C
 ClinVar gnomAD v4
2g.47414360A>GCA346732907MSH2c.884A>G (p.Asp295Gly)
c.686A>G (p.Asp229Gly)
n.956A>G
n.946A>G
 dbSNP
2g.47414360A>TCA346732908MSH2c.884A>T (p.Asp295Val)
c.686A>T (p.Asp229Val)
n.956A>T
n.946A>T
2g.47414361C>ACA346732909MSH2c.885C>A (p.Asp295Glu)
c.687C>A (p.Asp229Glu)
n.957C>A
n.947C>A
 dbSNP
2g.47414361C=CA2495834000MSH2c.885C= (p.Asp295=)
c.687C= (p.Asp229=)
n.957C=
n.947C=
2g.47414361C>GCA041012MSH2c.885C>G (p.Asp295Glu)
c.687C>G (p.Asp229Glu)
n.957C>G
n.947C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47414361C>TCA16604232MSH2c.885C>T (p.Asp295=)
c.687C>T (p.Asp229=)
n.957C>T
n.947C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched