Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.47411348_47413406delCA658760710MSH2c.645+976_792+846del
c.447+976_594+846del
n.717+976_864+846del
n.707+976_854+846del
2g.47412411_47412447dupCA2499215987MSH2c.646-3_679dup
c.448-3_481dup
n.718-3_751dup
n.708-3_741dup
 ClinVar dbSNP
2g.47412408_47412495delCA2580066592MSH2c.646-6_727del
c.448-6_529del
n.718-6_799del
n.708-6_789del
 ClinVar
2g.47412413_47413046delCA2499215988MSH2c.646-1_792+486del
c.448-1_594+486del
n.718-1_864+486del
n.708-1_854+486del
 ClinVar dbSNP
2g.47412433_47412456dupCA2580066622MSH2c.665_688dup (p.Lys229_Ala230insValLeuIleThrGluArgLysLys)
c.467_490dup (p.Lys163_Ala164insValLeuIleThrGluArgLysLys)
n.737_760dup
n.727_750dup
 ClinVar
2g.47412442_47412446delinsCAGAACA2495832689MSH2c.674_678delinsCAGAA (p.Thr225=)
c.476_480delinsCAGAA (p.Thr159=)
n.746_750delinsCAGAA
n.736_740delinsCAGAA
2g.47412442_47412447delinsCAGAAACA2495832688MSH2c.674_679delinsCAGAAA (p.Thr225=)
c.476_481delinsCAGAAA (p.Thr159=)
n.746_751delinsCAGAAA
n.736_741delinsCAGAAA
2g.47412443_47412447delinsTAATCA021733MSH2c.675_679delinsTAAT (p.Glu226AsnfsTer20)
c.477_481delinsTAAT (p.Glu160AsnfsTer20)
n.747_751delinsTAAT
n.737_741delinsTAAT
 ClinVar dbSNP
2g.47412448_47412451delCA021730MSH2c.680_683del (p.Arg227LysfsTer18)
c.482_485del (p.Arg161LysfsTer18)
n.752_755del
n.742_745del
 ClinVar dbSNP
2g.47412444_47412445delinsGACA2495832691MSH2c.676_677delinsGA (p.Glu226=)
c.478_479delinsGA (p.Glu160=)
n.748_749delinsGA
n.738_739delinsGA
2g.47412445A=CA2495832692MSH2c.677A= (p.Glu226=)
c.479A= (p.Glu160=)
n.749A=
n.739A=
2g.47412445A>CCA346731824MSH2c.677A>C (p.Glu226Ala)
c.479A>C (p.Glu160Ala)
n.749A>C
n.739A>C
2g.47412445A>GCA346731826MSH2c.677A>G (p.Glu226Gly)
c.479A>G (p.Glu160Gly)
n.749A>G
n.739A>G
 ClinVar dbSNP
2g.47412445A>TCA346731828MSH2c.677A>T (p.Glu226Val)
c.479A>T (p.Glu160Val)
n.749A>T
n.739A>T
2g.47412447dupCA2586969192MSH2c.679dup (p.Arg227LysfsTer5)
c.481dup (p.Arg161LysfsTer5)
n.751dup
n.741dup
2g.47412447delCA915943887MSH2c.679del (p.Arg227GlufsTer19)
c.481del (p.Arg161GlufsTer19)
n.751del
n.741del
 ClinVar dbSNP
2g.47412446A>CCA346731832MSH2c.678A>C (p.Glu226Asp)
c.480A>C (p.Glu160Asp)
n.750A>C
n.740A>C
2g.47412446A>GCA425967425MSH2c.678A>G (p.Glu226=)
c.480A>G (p.Glu160=)
n.750A>G
n.740A>G
2g.47412446A>TCA346731835MSH2c.678A>T (p.Glu226Asp)
c.480A>T (p.Glu160Asp)
n.750A>T
n.740A>T
 dbSNP
2g.47412446_47412448delinsAAGCA2495832693MSH2c.678_680delinsAAG (p.Glu226=)
c.480_482delinsAAG (p.Glu160=)
n.750_752delinsAAG
n.740_742delinsAAG
2g.47412447A=CA2495832694MSH2c.679A= (p.Arg227=)
c.481A= (p.Arg161=)
n.751A=
n.741A=
2g.47412447A>CCA425967429MSH2c.679A>C (p.Arg227=)
c.481A>C (p.Arg161=)
n.751A>C
n.741A>C
2g.47412447A>GCA040008MSH2c.679A>G (p.Arg227Gly)
c.481A>G (p.Arg161Gly)
n.751A>G
n.741A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47412447A>TCA346731838MSH2c.679A>T (p.Arg227Ter)
c.481A>T (p.Arg161Ter)
n.751A>T
n.741A>T
 ClinVar
2g.47412448_47412449delCA913187974MSH2c.680_681del (p.Arg227LysfsTer4)
c.482_483del (p.Arg161LysfsTer4)
n.752_753del
n.742_743del
 ClinVar dbSNP
2g.47412448delCA2580066636MSH2c.680del (p.Arg227LysfsTer19)
c.482del (p.Arg161LysfsTer19)
n.752del
n.742del
 ClinVar
2g.47412448G>ACA346731845MSH2c.680G>A (p.Arg227Lys)
c.482G>A (p.Arg161Lys)
n.752G>A
n.742G>A
 ClinVar
2g.47412448G>CCA346731847MSH2c.680G>C (p.Arg227Thr)
c.482G>C (p.Arg161Thr)
n.752G>C
n.742G>C
2g.47412448G>TCA346731849MSH2c.680G>T (p.Arg227Ile)
c.482G>T (p.Arg161Ile)
n.752G>T
n.742G>T
 ClinVar
2g.47412448dupCA2580612945MSH2c.680dup (p.Ala230SerfsTer2)
c.482dup (p.Ala164SerfsTer2)
n.752dup
n.742dup
 ClinVar
2g.47412448_47412450delinsGAACA2495832695MSH2c.680_682delinsGAA (p.Arg227=)
c.482_484delinsGAA (p.Arg161=)
n.752_754delinsGAA
n.742_744delinsGAA
2g.47412449A=CA2495832696MSH2c.681A= (p.Arg227=)
c.483A= (p.Arg161=)
n.753A=
n.743A=
2g.47412449A>CCA10577944MSH2c.681A>C (p.Arg227Ser)
c.483A>C (p.Arg161Ser)
n.753A>C
n.743A>C
 ClinVar dbSNP
2g.47412449A>GCA425967445MSH2c.681A>G (p.Arg227=)
c.483A>G (p.Arg161=)
n.753A>G
n.743A>G
2g.47412449A>TCA346731861MSH2c.681A>T (p.Arg227Ser)
c.483A>T (p.Arg161Ser)
n.753A>T
n.743A>T
 ClinVar dbSNP
2g.47412449_47412450delinsCCA2580066862MSH2c.681_682delinsC (p.Arg227SerfsTer19)
c.483_484delinsC (p.Arg161SerfsTer19)
n.753_754delinsC
n.743_744delinsC
 ClinVar
2g.47412455dupCA021991MSH2c.687dup (p.Ala230SerfsTer2)
c.489dup (p.Ala164SerfsTer2)
n.759dup
n.749dup
 ClinVar dbSNP gnomAD v4
2g.47412455delCA021998MSH2c.687del (p.Ala230LeufsTer16)
c.489del (p.Ala164LeufsTer16)
n.759del
n.749del
 ClinVar dbSNP gnomAD v4 COSMIC
2g.47412454_47412455delCA021960MSH2c.686_687del (p.Lys229SerfsTer2)
c.488_489del (p.Lys163SerfsTer2)
n.758_759del
n.748_749del
 ClinVar dbSNP
2g.47412452_47412455delCA2580066865MSH2c.684_687del (p.Lys229LeufsTer16)
c.486_489del (p.Lys163LeufsTer16)
n.756_759del
n.746_749del
 ClinVar
2g.47412449_47412457delinsGAAAAAGGCA2580066864MSH2c.681_689delinsGAAAAAGG (p.Ala230ValfsTer16)
c.483_491delinsGAAAAAGG (p.Ala164ValfsTer16)
n.753_761delinsGAAAAAGG
n.743_751delinsGAAAAAGG
 ClinVar
2g.47412450A=CA2495832697MSH2c.682A= (p.Lys228=)
c.484A= (p.Lys162=)
n.754A=
n.744A=
2g.47412450A>CCA346731864MSH2c.682A>C (p.Lys228Gln)
c.484A>C (p.Lys162Gln)
n.754A>C
n.744A>C
 gnomAD v4
2g.47412450A>GCA040044MSH2c.682A>G (p.Lys228Glu)
c.484A>G (p.Lys162Glu)
n.754A>G
n.744A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412450A>TCA346731867MSH2c.682A>T (p.Lys228Ter)
c.484A>T (p.Lys162Ter)
n.754A>T
n.744A>T
 dbSNP
2g.47412451A>CCA346731874MSH2c.683A>C (p.Lys228Thr)
c.485A>C (p.Lys162Thr)
n.755A>C
n.745A>C
2g.47412451A>GCA346731875MSH2c.683A>G (p.Lys228Arg)
c.485A>G (p.Lys162Arg)
n.755A>G
n.745A>G
2g.47412451A>TCA346731871MSH2c.683A>T (p.Lys228Ile)
c.485A>T (p.Lys162Ile)
n.755A>T
n.745A>T
2g.47412452A>CCA346731876MSH2c.684A>C (p.Lys228Asn)
c.486A>C (p.Lys162Asn)
n.756A>C
n.746A>C
2g.47412452A>GCA425967472MSH2c.684A>G (p.Lys228=)
c.486A>G (p.Lys162=)
n.756A>G
n.746A>G
2g.47412452A>TCA346731877MSH2c.684A>T (p.Lys228Asn)
c.486A>T (p.Lys162Asn)
n.756A>T
n.746A>T
 dbSNP
2g.47412453A=CA2495832698MSH2c.685A= (p.Lys229=)
c.487A= (p.Lys163=)
n.757A=
n.747A=
2g.47412453A>CCA346731878MSH2c.685A>C (p.Lys229Gln)
c.487A>C (p.Lys163Gln)
n.757A>C
n.747A>C
2g.47412453A>GCA346731880MSH2c.685A>G (p.Lys229Glu)
c.487A>G (p.Lys163Glu)
n.757A>G
n.747A>G
2g.47412453A>TCA021947MSH2c.685A>T (p.Lys229Ter)
c.487A>T (p.Lys163Ter)
n.757A>T
n.747A>T
 ClinVar dbSNP
2g.47412454A>CCA346731887MSH2c.686A>C (p.Lys229Thr)
c.488A>C (p.Lys163Thr)
n.758A>C
n.748A>C
2g.47412454A>GCA346731886MSH2c.686A>G (p.Lys229Arg)
c.488A>G (p.Lys163Arg)
n.758A>G
n.748A>G
2g.47412454A>TCA346731884MSH2c.686A>T (p.Lys229Ile)
c.488A>T (p.Lys163Ile)
n.758A>T
n.748A>T
 ClinVar dbSNP
2g.47412454_47412455insTGAAAATTATAACATTGATAACTATCA2699268402MSH2c.686_687insTGAAAATTATAACATTGATAACTAT (p.Lys229AsnfsTer11)
c.488_489insTGAAAATTATAACATTGATAACTAT (p.Lys163AsnfsTer11)
n.758_759insTGAAAATTATAACATTGATAACTAT
n.748_749insTGAAAATTATAACATTGATAACTAT
 dbSNP
2g.47412455A=CA2495832699MSH2c.687A= (p.Lys229=)
c.489A= (p.Lys163=)
n.759A=
n.749A=
2g.47412455A>CCA346731890MSH2c.687A>C (p.Lys229Asn)
c.489A>C (p.Lys163Asn)
n.759A>C
n.749A>C
2g.47412455A>GCA425967492MSH2c.687A>G (p.Lys229=)
c.489A>G (p.Lys163=)
n.759A>G
n.749A>G
 ClinVar gnomAD v4
2g.47412455A>TCA346731892MSH2c.687A>T (p.Lys229Asn)
c.489A>T (p.Lys163Asn)
n.759A>T
n.749A>T
 gnomAD v4
2g.47412455_47412456insTCA645369190MSH2c.687_688insT (p.Ala230CysfsTer2)
c.489_490insT (p.Ala164CysfsTer2)
n.759_760insT
n.749_750insT
 ClinVar dbSNP
2g.47412456G>ACA346731895MSH2c.688G>A (p.Ala230Thr)
c.490G>A (p.Ala164Thr)
n.760G>A
n.750G>A
 ClinVar dbSNP gnomAD v4
2g.47412456G>CCA346731898MSH2c.688G>C (p.Ala230Pro)
c.490G>C (p.Ala164Pro)
n.760G>C
n.750G>C
 ClinVar dbSNP
2g.47412456G=CA2495832700MSH2c.688G= (p.Ala230=)
c.490G= (p.Ala164=)
n.760G=
n.750G=
2g.47412456G>TCA346731899MSH2c.688G>T (p.Ala230Ser)
c.490G>T (p.Ala164Ser)
n.760G>T
n.750G>T
 ClinVar dbSNP
2g.47412457delCA2580066872MSH2c.689del (p.Ala230ValfsTer16)
c.491del (p.Ala164ValfsTer16)
n.761del
n.751del
 ClinVar
2g.47412457C>ACA346731907MSH2c.689C>A (p.Ala230Asp)
c.491C>A (p.Ala164Asp)
n.761C>A
n.751C>A
 ClinVar dbSNP gnomAD v4
2g.47412457C=CA2495832701MSH2c.689C= (p.Ala230=)
c.491C= (p.Ala164=)
n.761C=
n.751C=
2g.47412457C>GCA346731904MSH2c.689C>G (p.Ala230Gly)
c.491C>G (p.Ala164Gly)
n.761C>G
n.751C>G
 ClinVar dbSNP
2g.47412457C>TCA346731902MSH2c.689C>T (p.Ala230Val)
c.491C>T (p.Ala164Val)
n.761C>T
n.751C>T
 ClinVar dbSNP gnomAD v4
2g.47412457_47412459delinsTTCA2586969194MSH2c.689_691delinsTT (p.Ala230ValfsTer16)
c.491_493delinsTT (p.Ala164ValfsTer16)
n.761_763delinsTT
n.751_753delinsTT
2g.47412458T>ACA425967509MSH2c.690T>A (p.Ala230=)
c.492T>A (p.Ala164=)
n.762T>A
n.752T>A
 dbSNP
2g.47412458T>CCA425967512MSH2c.690T>C (p.Ala230=)
c.492T>C (p.Ala164=)
n.762T>C
n.752T>C
 ClinVar dbSNP gnomAD v4 COSMIC
2g.47412458T>GCA425967506MSH2c.690T>G (p.Ala230=)
c.492T>G (p.Ala164=)
n.762T>G
n.752T>G
2g.47412458T=CA2495832703MSH2c.690T= (p.Ala230=)
c.492T= (p.Ala164=)
n.762T=
n.752T=
2g.47412458_47412459delinsTGCA2495832702MSH2c.690_691delinsTG (p.Ala230=)
c.492_493delinsTG (p.Ala164=)
n.762_763delinsTG
n.752_753delinsTG
2g.47412458_47412460delCA2697548109MSH2c.690_692del (p.Asp231del)
c.492_494del (p.Asp165del)
n.762_764del
n.752_754del
 ClinVar
2g.47412458_47412461delinsCTCA2831039063MSH2c.690_693delinsCT (p.Asp231PhefsTer24)
c.492_495delinsCT (p.Asp165PhefsTer24)
n.762_765delinsCT
n.752_755delinsCT
2g.47412459delCA022028MSH2c.691del (p.Asp231ThrfsTer15)
c.493del (p.Asp165ThrfsTer15)
n.763del
n.753del
 ClinVar dbSNP
2g.47412459G>ACA346731911MSH2c.691G>A (p.Asp231Asn)
c.493G>A (p.Asp165Asn)
n.763G>A
n.753G>A
 ClinVar dbSNP gnomAD v4
2g.47412459G>CCA346731914MSH2c.691G>C (p.Asp231His)
c.493G>C (p.Asp165His)
n.763G>C
n.753G>C
 dbSNP gnomAD v3 gnomAD v4
2g.47412459G=CA2495832704MSH2c.691G= (p.Asp231=)
c.493G= (p.Asp165=)
n.763G=
n.753G=
2g.47412459G>TCA346731917MSH2c.691G>T (p.Asp231Tyr)
c.493G>T (p.Asp165Tyr)
n.763G>T
n.753G>T
 ClinVar dbSNP gnomAD v4
2g.47412460A>CCA346731928MSH2c.692A>C (p.Asp231Ala)
c.494A>C (p.Asp165Ala)
n.764A>C
n.754A>C
2g.47412460A>GCA346731930MSH2c.692A>G (p.Asp231Gly)
c.494A>G (p.Asp165Gly)
n.764A>G
n.754A>G
 gnomAD v4
2g.47412460A>TCA346731932MSH2c.692A>T (p.Asp231Val)
c.494A>T (p.Asp165Val)
n.764A>T
n.754A>T
 dbSNP
2g.47412461C>ACA346731937MSH2c.693C>A (p.Asp231Glu)
c.495C>A (p.Asp165Glu)
n.765C>A
n.755C>A
2g.47412461C=CA2495832706MSH2c.693C= (p.Asp231=)
c.495C= (p.Asp165=)
n.765C=
n.755C=
2g.47412461C>GCA346731939MSH2c.693C>G (p.Asp231Glu)
c.495C>G (p.Asp165Glu)
n.765C>G
n.755C>G
 dbSNP
2g.47412461C>TCA040060MSH2c.693C>T (p.Asp231=)
c.495C>T (p.Asp165=)
n.765C>T
n.755C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412461_47412463delinsCTTCA2495832705MSH2c.693_695delinsCTT (p.Asp231=)
c.495_497delinsCTT (p.Asp165=)
n.765_767delinsCTT
n.755_757delinsCTT
2g.47412462T>ACA346731946MSH2c.694T>A (p.Phe232Ile)
c.496T>A (p.Phe166Ile)
n.766T>A
n.756T>A
2g.47412462T>CCA346731951MSH2c.694T>C (p.Phe232Leu)
c.496T>C (p.Phe166Leu)
n.766T>C
n.756T>C
2g.47412462T>GCA346731949MSH2c.694T>G (p.Phe232Val)
c.496T>G (p.Phe166Val)
n.766T>G
n.756T>G
2g.47412465dupCA2697548110MSH2c.697dup (p.Ser233PhefsTer23)
c.499dup (p.Ser167PhefsTer23)
n.769dup
n.759dup
 ClinVar
2g.47412465delCA2499215990MSH2c.697del (p.Ser233ProfsTer13)
c.499del (p.Ser167ProfsTer13)
n.769del
n.759del
 ClinVar dbSNP
2g.47412464_47412465delCA022033MSH2c.696_697del (p.Ser233HisfsTer22)
c.498_499del (p.Ser167HisfsTer22)
n.768_769del
n.758_759del
 ClinVar dbSNP
2g.47412463T>ACA346731955MSH2c.695T>A (p.Phe232Tyr)
c.497T>A (p.Phe166Tyr)
n.767T>A
n.757T>A
2g.47412463T>CCA346731957MSH2c.695T>C (p.Phe232Ser)
c.497T>C (p.Phe166Ser)
n.767T>C
n.757T>C
 dbSNP gnomAD v4
2g.47412463T>GCA346731961MSH2c.695T>G (p.Phe232Cys)
c.497T>G (p.Phe166Cys)
n.767T>G
n.757T>G
2g.47412464T>ACA346731964MSH2c.696T>A (p.Phe232Leu)
c.498T>A (p.Phe166Leu)
n.768T>A
n.758T>A
2g.47412464T>CCA425967560MSH2c.696T>C (p.Phe232=)
c.498T>C (p.Phe166=)
n.768T>C
n.758T>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47412464T>GCA346731966MSH2c.696T>G (p.Phe232Leu)
c.498T>G (p.Phe166Leu)
n.768T>G
n.758T>G
2g.47412464T=CA2495832707MSH2c.696T= (p.Phe232=)
c.498T= (p.Phe166=)
n.768T=
n.758T=
2g.47412465T>ACA346731976MSH2c.697T>A (p.Ser233Thr)
c.499T>A (p.Ser167Thr)
n.769T>A
n.759T>A
2g.47412465T>CCA346731973MSH2c.697T>C (p.Ser233Pro)
c.499T>C (p.Ser167Pro)
n.769T>C
n.759T>C
 gnomAD v4
2g.47412465T>GCA346731969MSH2c.697T>G (p.Ser233Ala)
c.499T>G (p.Ser167Ala)
n.769T>G
n.759T>G
2g.47412466C>ACA346731980MSH2c.698C>A (p.Ser233Tyr)
c.500C>A (p.Ser167Tyr)
n.770C>A
n.760C>A
 dbSNP
2g.47412466C=CA2495832708MSH2c.698C= (p.Ser233=)
c.500C= (p.Ser167=)
n.770C=
n.760C=
2g.47412466C>GCA022041MSH2c.698C>G (p.Ser233Cys)
c.500C>G (p.Ser167Cys)
n.770C>G
n.760C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47412466C>TCA346731983MSH2c.698C>T (p.Ser233Phe)
c.500C>T (p.Ser167Phe)
n.770C>T
n.760C>T
 ClinVar dbSNP gnomAD v4
2g.47412467delCA1139771116MSH2c.699del (p.Thr234GlnfsTer12)
c.501del (p.Thr168GlnfsTer12)
n.771del
n.761del
 ClinVar
2g.47412466_47412484delinsCCACAAAAGACATTTATCACA2495832709MSH2c.698_716delinsCCACAAAAGACATTTATCA (p.Ser233=)
c.500_518delinsCCACAAAAGACATTTATCA (p.Ser167=)
n.770_788delinsCCACAAAAGACATTTATCA
n.760_778delinsCCACAAAAGACATTTATCA
2g.47412467C>ACA425967576MSH2c.699C>A (p.Ser233=)
c.501C>A (p.Ser167=)
n.771C>A
n.761C>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.47412467C=CA2495832711MSH2c.699C= (p.Ser233=)
c.501C= (p.Ser167=)
n.771C=
n.761C=
2g.47412467C>GCA425967578MSH2c.699C>G (p.Ser233=)
c.501C>G (p.Ser167=)
n.771C>G
n.761C>G
2g.47412467C>TCA425967581MSH2c.699C>T (p.Ser233=)
c.501C>T (p.Ser167=)
n.771C>T
n.761C>T
 dbSNP gnomAD v4 COSMIC
2g.47412467_47412484delCA2495832710MSH2c.699_716del (p.Thr234_Gln239del)
c.501_518del (p.Thr168_Gln173del)
n.771_788del
n.761_778del
 ClinVar dbSNP
2g.47412468A=CA2495832712MSH2c.700A= (p.Thr234=)
c.502A= (p.Thr168=)
n.772A=
n.762A=
2g.47412468A>CCA346731984MSH2c.700A>C (p.Thr234Pro)
c.502A>C (p.Thr168Pro)
n.772A>C
n.762A>C
2g.47412468A>GCA346731985MSH2c.700A>G (p.Thr234Ala)
c.502A>G (p.Thr168Ala)
n.772A>G
n.762A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47412468A>TCA346731986MSH2c.700A>T (p.Thr234Ser)
c.502A>T (p.Thr168Ser)
n.772A>T
n.762A>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47412471_47412477delCA2499215991MSH2c.703_709del (p.Lys235PhefsTer9)
c.505_511del (p.Lys169PhefsTer9)
n.775_781del
n.765_771del
 ClinVar dbSNP
2g.47412469C>ACA346731989MSH2c.701C>A (p.Thr234Lys)
c.503C>A (p.Thr168Lys)
n.773C>A
n.763C>A
 ClinVar
2g.47412469C=CA2495832714MSH2c.701C= (p.Thr234=)
c.503C= (p.Thr168=)
n.773C=
n.763C=
2g.47412469C>GCA10577945MSH2c.701C>G (p.Thr234Arg)
c.503C>G (p.Thr168Arg)
n.773C>G
n.763C>G
 ClinVar dbSNP
2g.47412469C>TCA022053MSH2c.701C>T (p.Thr234Ile)
c.503C>T (p.Thr168Ile)
n.773C>T
n.763C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.47412469_47412471delinsCAACA2495832713MSH2c.701_703delinsCAA (p.Thr234=)
c.503_505delinsCAA (p.Thr168=)
n.773_775delinsCAA
n.763_765delinsCAA
2g.47412470A=CA2495832715MSH2c.702A= (p.Thr234=)
c.504A= (p.Thr168=)
n.774A=
n.764A=
2g.47412470A>CCA425967595MSH2c.702A>C (p.Thr234=)
c.504A>C (p.Thr168=)
n.774A>C
n.764A>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47412470A>GCA040148MSH2c.702A>G (p.Thr234=)
c.504A>G (p.Thr168=)
n.774A>G
n.764A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412470A>TCA425967599MSH2c.702A>T (p.Thr234=)
c.504A>T (p.Thr168=)
n.774A>T
n.764A>T
 gnomAD v4
2g.47412473delCA022063MSH2c.705del (p.Asp236ThrfsTer10)
c.507del (p.Asp170ThrfsTer10)
n.777del
n.767del
 ClinVar dbSNP
2g.47412472_47412473delCA022059MSH2c.704_705del (p.Lys235ArgfsTer20)
c.506_507del (p.Lys169ArgfsTer20)
n.776_777del
n.766_767del
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47412471A=CA2495832716MSH2c.703A= (p.Lys235=)
c.505A= (p.Lys169=)
n.775A=
n.765A=
2g.47412471A>CCA346732005MSH2c.703A>C (p.Lys235Gln)
c.505A>C (p.Lys169Gln)
n.775A>C
n.765A>C
2g.47412471A>GCA040162MSH2c.703A>G (p.Lys235Glu)
c.505A>G (p.Lys169Glu)
n.775A>G
n.765A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412471A>TCA346732002MSH2c.703A>T (p.Lys235Ter)
c.505A>T (p.Lys169Ter)
n.775A>T
n.765A>T
2g.47412472A>CCA346732011MSH2c.704A>C (p.Lys235Thr)
c.506A>C (p.Lys169Thr)
n.776A>C
n.766A>C
 ClinVar dbSNP
2g.47412472A>GCA346732013MSH2c.704A>G (p.Lys235Arg)
c.506A>G (p.Lys169Arg)
n.776A>G
n.766A>G
2g.47412472A>TCA346732017MSH2c.704A>T (p.Lys235Ile)
c.506A>T (p.Lys169Ile)
n.776A>T
n.766A>T
2g.47412473A>CCA346732020MSH2c.705A>C (p.Lys235Asn)
c.507A>C (p.Lys169Asn)
n.777A>C
n.767A>C
2g.47412473A>GCA425967624MSH2c.705A>G (p.Lys235=)
c.507A>G (p.Lys169=)
n.777A>G
n.767A>G
2g.47412473A>TCA346732023MSH2c.705A>T (p.Lys235Asn)
c.507A>T (p.Lys169Asn)
n.777A>T
n.767A>T
 dbSNP
2g.47412474G>ACA346732026MSH2c.706G>A (p.Asp236Asn)
c.508G>A (p.Asp170Asn)
n.778G>A
n.768G>A
 ClinVar dbSNP
2g.47412474G>CCA16617560MSH2c.706G>C (p.Asp236His)
c.508G>C (p.Asp170His)
n.778G>C
n.768G>C
 ClinVar dbSNP
2g.47412474G=CA2495832717MSH2c.706G= (p.Asp236=)
c.508G= (p.Asp170=)
n.778G=
n.768G=
2g.47412474G>TCA346732029MSH2c.706G>T (p.Asp236Tyr)
c.508G>T (p.Asp170Tyr)
n.778G>T
n.768G>T
 ClinVar
2g.47412475A=CA2495832719MSH2c.707A= (p.Asp236=)
c.509A= (p.Asp170=)
n.779A=
n.769A=
2g.47412475A>CCA346732033MSH2c.707A>C (p.Asp236Ala)
c.509A>C (p.Asp170Ala)
n.779A>C
n.769A>C
 dbSNP
2g.47412475A>GCA10577946MSH2c.707A>G (p.Asp236Gly)
c.509A>G (p.Asp170Gly)
n.779A>G
n.769A>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47412475A>TCA346732037MSH2c.707A>T (p.Asp236Val)
c.509A>T (p.Asp170Val)
n.779A>T
n.769A>T
 dbSNP
2g.47412475_47412482delinsACATTTATCA2495832718MSH2c.707_714delinsACATTTAT (p.Asp236=)
c.509_516delinsACATTTAT (p.Asp170=)
n.779_786delinsACATTTAT
n.769_776delinsACATTTAT
2g.47412476C>ACA346732040MSH2c.708C>A (p.Asp236Glu)
c.510C>A (p.Asp170Glu)
n.780C>A
n.770C>A
 ClinVar dbSNP
2g.47412476C=CA2495832721MSH2c.708C= (p.Asp236=)
c.510C= (p.Asp170=)
n.780C=
n.770C=
2g.47412476C>GCA346732045MSH2c.708C>G (p.Asp236Glu)
c.510C>G (p.Asp170Glu)
n.780C>G
n.770C>G
 ClinVar dbSNP
2g.47412476C>TCA425967640MSH2c.708C>T (p.Asp236=)
c.510C>T (p.Asp170=)
n.780C>T
n.770C>T
 ClinVar dbSNP
2g.47412476_47412480delinsCATTTCA2495832720MSH2c.708_712delinsCATTT (p.Asp236=)
c.510_514delinsCATTT (p.Asp170=)
n.780_784delinsCATTT
n.770_774delinsCATTT
2g.47412478_47412484delCA645369191MSH2c.710_716del (p.Ile237ArgfsTer7)
c.512_518del (p.Ile171ArgfsTer7)
n.782_788del
n.772_778del
 ClinVar dbSNP
2g.47412477delCA2580066887MSH2c.709del (p.Ile237PhefsTer9)
c.511del (p.Ile171PhefsTer9)
n.781del
n.771del
 ClinVar
2g.47412477A=CA2495832722MSH2c.709A= (p.Ile237=)
c.511A= (p.Ile171=)
n.781A=
n.771A=
2g.47412477A>CCA346732052MSH2c.709A>C (p.Ile237Leu)
c.511A>C (p.Ile171Leu)
n.781A>C
n.771A>C
2g.47412477A>GCA022070MSH2c.709A>G (p.Ile237Val)
c.511A>G (p.Ile171Val)
n.781A>G
n.771A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
2g.47412477A>TCA346732051MSH2c.709A>T (p.Ile237Phe)
c.511A>T (p.Ile171Phe)
n.781A>T
n.771A>T
 ClinVar dbSNP
2g.47412479_47412482dupCA891841777MSH2c.711_714dup (p.Gln239LeufsTer18)
c.513_516dup (p.Gln173LeufsTer18)
n.783_786dup
n.773_776dup
2g.47412479_47412482delCA022080MSH2c.711_714del (p.Tyr238ArgfsTer7)
c.513_516del (p.Tyr172ArgfsTer7)
n.783_786del
n.773_776del
 ClinVar dbSNP
2g.47412478T>ACA346732053MSH2c.710T>A (p.Ile237Asn)
c.512T>A (p.Ile171Asn)
n.782T>A
n.772T>A
 dbSNP
2g.47412478T>CCA346732055MSH2c.710T>C (p.Ile237Thr)
c.512T>C (p.Ile171Thr)
n.782T>C
n.772T>C
2g.47412478T>GCA346732057MSH2c.710T>G (p.Ile237Ser)
c.512T>G (p.Ile171Ser)
n.782T>G
n.772T>G
 ClinVar
2g.47412480delCA2580066888MSH2c.712del (p.Tyr238IlefsTer8)
c.514del (p.Tyr172IlefsTer8)
n.784del
n.774del
 ClinVar
2g.47412478_47412483delinsAAAGGTTCCACAAACA2580066889MSH2c.710_715delinsAAAGGTTCCACAAA (p.Ile237LysfsTer12)
c.512_517delinsAAAGGTTCCACAAA (p.Ile171LysfsTer12)
n.782_787delinsAAAGGTTCCACAAA
n.772_777delinsAAAGGTTCCACAAA
 ClinVar
2g.47412479T>ACA425967648MSH2c.711T>A (p.Ile237=)
c.513T>A (p.Ile171=)
n.783T>A
n.773T>A
 dbSNP
2g.47412479T>CCA425967650MSH2c.711T>C (p.Ile237=)
c.513T>C (p.Ile171=)
n.783T>C
n.773T>C
 ClinVar dbSNP
2g.47412479T>GCA346732061MSH2c.711T>G (p.Ile237Met)
c.513T>G (p.Ile171Met)
n.783T>G
n.773T>G
2g.47412479_47412495delCA658760732MSH2c.711_727del (p.Ile237MetfsTer13)
c.513_529del (p.Ile171MetfsTer13)
n.783_799del
n.773_789del
2g.47412480T>ACA346732068MSH2c.712T>A (p.Tyr238Asn)
c.514T>A (p.Tyr172Asn)
n.784T>A
n.774T>A
 dbSNP
2g.47412480T>CCA346732066MSH2c.712T>C (p.Tyr238His)
c.514T>C (p.Tyr172His)
n.784T>C
n.774T>C
 ClinVar
2g.47412480T>GCA16611002MSH2c.712T>G (p.Tyr238Asp)
c.514T>G (p.Tyr172Asp)
n.784T>G
n.774T>G
 ClinVar dbSNP gnomAD v4
2g.47412480T=CA2495832723MSH2c.712T= (p.Tyr238=)
c.514T= (p.Tyr172=)
n.784T=
n.774T=
2g.47412481A=CA2495832724MSH2c.713A= (p.Tyr238=)
c.515A= (p.Tyr172=)
n.785A=
n.775A=
2g.47412481A>CCA346732070MSH2c.713A>C (p.Tyr238Ser)
c.515A>C (p.Tyr172Ser)
n.785A>C
n.775A>C
2g.47412481A>GCA346732073MSH2c.713A>G (p.Tyr238Cys)
c.515A>G (p.Tyr172Cys)
n.785A>G
n.775A>G
 ClinVar dbSNP gnomAD v4
2g.47412481A>TCA346732076MSH2c.713A>T (p.Tyr238Phe)
c.515A>T (p.Tyr172Phe)
n.785A>T
n.775A>T
 ClinVar dbSNP
2g.47412482_47412487delCA2658946232MSH2c.714_719del (p.Gln239_Asp240del)
c.516_521del (p.Gln173_Asp174del)
n.786_791del
n.776_781del
 gnomAD v4
2g.47412482T>ACA346732079MSH2c.714T>A (p.Tyr238Ter)
c.516T>A (p.Tyr172Ter)
n.786T>A
n.776T>A
 dbSNP
2g.47412482T>CCA040171MSH2c.714T>C (p.Tyr238=)
c.516T>C (p.Tyr172=)
n.786T>C
n.776T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412482T>GCA346732082MSH2c.714T>G (p.Tyr238Ter)
c.516T>G (p.Tyr172Ter)
n.786T>G
n.776T>G
 ClinVar dbSNP
2g.47412482T=CA2495832725MSH2c.714T= (p.Tyr238=)
c.516T= (p.Tyr172=)
n.786T=
n.776T=
2g.47412483C>ACA346732084MSH2c.715C>A (p.Gln239Lys)
c.517C>A (p.Gln173Lys)
n.787C>A
n.777C>A
2g.47412483C=CA2495832726MSH2c.715C= (p.Gln239=)
c.517C= (p.Gln173=)
n.787C=
n.777C=
2g.47412483C>GCA16610793MSH2c.715C>G (p.Gln239Glu)
c.517C>G (p.Gln173Glu)
n.787C>G
n.777C>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47412483C>TCA022086MSH2c.715C>T (p.Gln239Ter)
c.517C>T (p.Gln173Ter)
n.787C>T
n.777C>T
 ClinVar dbSNP
2g.47412483dupCA2695200765MSH2c.715dup (p.Gln239ProfsTer17)
c.517dup (p.Gln173ProfsTer17)
n.787dup
n.777dup
 ClinVar
2g.47412484A=CA2495832728MSH2c.716A= (p.Gln239=)
c.518A= (p.Gln173=)
n.788A=
n.778A=
2g.47412484A>CCA346732090MSH2c.716A>C (p.Gln239Pro)
c.518A>C (p.Gln173Pro)
n.788A>C
n.778A>C
 ClinVar dbSNP
2g.47412484A>GCA022091MSH2c.716A>G (p.Gln239Arg)
c.518A>G (p.Gln173Arg)
n.788A>G
n.778A>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.47412484A>TCA346732096MSH2c.716A>T (p.Gln239Leu)
c.518A>T (p.Gln173Leu)
n.788A>T
n.778A>T
 ClinVar dbSNP
2g.47412484_47412489delinsAGGACCCA2495832727MSH2c.716_721delinsAGGACC (p.Gln239=)
c.518_523delinsAGGACC (p.Gln173=)
n.788_793delinsAGGACC
n.778_783delinsAGGACC
2g.47412485G>ACA425967683MSH2c.717G>A (p.Gln239=)
c.519G>A (p.Gln173=)
n.789G>A
n.779G>A
 dbSNP
2g.47412485G>CCA346732111MSH2c.717G>C (p.Gln239His)
c.519G>C (p.Gln173His)
n.789G>C
n.779G>C
 ClinVar dbSNP
2g.47412485G>TCA346732113MSH2c.717G>T (p.Gln239His)
c.519G>T (p.Gln173His)
n.789G>T
n.779G>T
 ClinVar dbSNP
2g.47412486delCA645531412MSH2c.718del (p.Asp240ThrfsTer6)
c.520del (p.Asp174ThrfsTer6)
n.790del
n.780del
 ClinVar dbSNP COSMIC
2g.47412485_47412489delinsTTACA022098MSH2c.717_721delinsTTA (p.Gln239HisfsTer16)
c.519_523delinsTTA (p.Gln173HisfsTer16)
n.789_793delinsTTA
n.779_783delinsTTA
 ClinVar dbSNP
2g.47412486G>ACA346732114MSH2c.718G>A (p.Asp240Asn)
c.520G>A (p.Asp174Asn)
n.790G>A
n.780G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47412486G>CCA346732117MSH2c.718G>C (p.Asp240His)
c.520G>C (p.Asp174His)
n.790G>C
n.780G>C
 dbSNP
2g.47412486G=CA2495832729MSH2c.718G= (p.Asp240=)
c.520G= (p.Asp174=)
n.790G=
n.780G=
2g.47412486G>TCA346732120MSH2c.718G>T (p.Asp240Tyr)
c.520G>T (p.Asp174Tyr)
n.790G>T
n.780G>T
 ClinVar dbSNP
2g.47412487A=CA2495832730MSH2c.719A= (p.Asp240=)
c.521A= (p.Asp174=)
n.791A=
n.781A=
2g.47412487A>CCA346732123MSH2c.719A>C (p.Asp240Ala)
c.521A>C (p.Asp174Ala)
n.791A>C
n.781A>C
 ClinVar dbSNP
2g.47412487A>GCA10582000MSH2c.719A>G (p.Asp240Gly)
c.521A>G (p.Asp174Gly)
n.791A>G
n.781A>G
 ClinVar dbSNP
2g.47412487A>TCA346732126MSH2c.719A>T (p.Asp240Val)
c.521A>T (p.Asp174Val)
n.791A>T
n.781A>T
 dbSNP
2g.47412487_47412488delinsACCA2495832731MSH2c.719_720delinsAC (p.Asp240=)
c.521_522delinsAC (p.Asp174=)
n.791_792delinsAC
n.781_782delinsAC
2g.47412488C>ACA346732133MSH2c.720C>A (p.Asp240Glu)
c.522C>A (p.Asp174Glu)
n.792C>A
n.782C>A
 dbSNP
2g.47412488C=CA2495832732MSH2c.720C= (p.Asp240=)
c.522C= (p.Asp174=)
n.792C=
n.782C=
2g.47412488C>GCA346732131MSH2c.720C>G (p.Asp240Glu)
c.522C>G (p.Asp174Glu)
n.792C>G
n.782C>G
 dbSNP
2g.47412488C>TCA425967697MSH2c.720C>T (p.Asp240=)
c.522C>T (p.Asp174=)
n.792C>T
n.782C>T
 ClinVar dbSNP
2g.47412489delCA915943888MSH2c.721del (p.Leu241SerfsTer5)
c.523del (p.Leu175SerfsTer5)
n.793del
n.783del
 ClinVar dbSNP
2g.47412489C>ACA346732136MSH2c.721C>A (p.Leu241Ile)
c.523C>A (p.Leu175Ile)
n.793C>A
n.783C>A
 ClinVar dbSNP
2g.47412489C=CA2495832733MSH2c.721C= (p.Leu241=)
c.523C= (p.Leu175=)
n.793C=
n.783C=
2g.47412489C>GCA346732141MSH2c.721C>G (p.Leu241Val)
c.523C>G (p.Leu175Val)
n.793C>G
n.783C>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47412489C>TCA346732138MSH2c.721C>T (p.Leu241Phe)
c.523C>T (p.Leu175Phe)
n.793C>T
n.783C>T
 ClinVar dbSNP gnomAD v4
2g.47412490T>ACA346732144MSH2c.722T>A (p.Leu241His)
c.524T>A (p.Leu175His)
n.794T>A
n.784T>A
 dbSNP
2g.47412490T>CCA346732149MSH2c.722T>C (p.Leu241Pro)
c.524T>C (p.Leu175Pro)
n.794T>C
n.784T>C
 ClinVar dbSNP
2g.47412490T>GCA346732146MSH2c.722T>G (p.Leu241Arg)
c.524T>G (p.Leu175Arg)
n.794T>G
n.784T>G
2g.47412491delCA2580066898MSH2c.723del (p.Asn242ThrfsTer4)
c.525del (p.Asn176ThrfsTer4)
n.795del
n.785del
 ClinVar
2g.47412491C>ACA425967710MSH2c.723C>A (p.Leu241=)
c.525C>A (p.Leu175=)
n.795C>A
n.785C>A
 dbSNP
2g.47412491C=CA2495832734MSH2c.723C= (p.Leu241=)
c.525C= (p.Leu175=)
n.795C=
n.785C=
2g.47412491C>GCA425967712MSH2c.723C>G (p.Leu241=)
c.525C>G (p.Leu175=)
n.795C>G
n.785C>G
 dbSNP
2g.47412491C>TCA425967714MSH2c.723C>T (p.Leu241=)
c.525C>T (p.Leu175=)
n.795C>T
n.785C>T
 ClinVar dbSNP gnomAD v4
2g.47412492A=CA2495832735MSH2c.724A= (p.Asn242=)
c.526A= (p.Asn176=)
n.796A=
n.786A=
2g.47412492A>CCA346732152MSH2c.724A>C (p.Asn242His)
c.526A>C (p.Asn176His)
n.796A>C
n.786A>C
 ClinVar dbSNP gnomAD v4
2g.47412492A>GCA346732159MSH2c.724A>G (p.Asn242Asp)
c.526A>G (p.Asn176Asp)
n.796A>G
n.786A>G
2g.47412492A>TCA346732155MSH2c.724A>T (p.Asn242Tyr)
c.526A>T (p.Asn176Tyr)
n.796A>T
n.786A>T
 dbSNP
2g.47412493dupCA331668MSH2c.725dup (p.Asn242LysfsTer14)
c.527dup (p.Asn176LysfsTer14)
n.797dup
n.787dup
 ClinVar dbSNP
2g.47412493A=CA2495832736MSH2c.725A= (p.Asn242=)
c.527A= (p.Asn176=)
n.797A=
n.787A=
2g.47412493A>CCA346732162MSH2c.725A>C (p.Asn242Thr)
c.527A>C (p.Asn176Thr)
n.797A>C
n.787A>C
 ClinVar dbSNP
2g.47412493A>GCA040185MSH2c.725A>G (p.Asn242Ser)
c.527A>G (p.Asn176Ser)
n.797A>G
n.787A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47412493A>TCA346732164MSH2c.725A>T (p.Asn242Ile)
c.527A>T (p.Asn176Ile)
n.797A>T
n.787A>T
 dbSNP
2g.47412494C>ACA346732169MSH2c.726C>A (p.Asn242Lys)
c.528C>A (p.Asn176Lys)
n.798C>A
n.788C>A
 ClinVar dbSNP
2g.47412494C=CA2495832737MSH2c.726C= (p.Asn242=)
c.528C= (p.Asn176=)
n.798C=
n.788C=
2g.47412494C>GCA16611006MSH2c.726C>G (p.Asn242Lys)
c.528C>G (p.Asn176Lys)
n.798C>G
n.788C>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47412494C>TCA040200MSH2c.726C>T (p.Asn242=)
c.528C>T (p.Asn176=)
n.798C>T
n.788C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412495delCA2580066900MSH2c.727del (p.Arg243GlyfsTer3)
c.529del (p.Arg177GlyfsTer3)
n.799del
n.789del
 ClinVar
2g.47412495C>ACA425967731MSH2c.727C>A (p.Arg243=)
c.529C>A (p.Arg177=)
n.799C>A
n.789C>A
 ClinVar dbSNP
2g.47412495C=CA2495832738MSH2c.727C= (p.Arg243=)
c.529C= (p.Arg177=)
n.799C=
n.789C=
2g.47412495C>GCA346732174MSH2c.727C>G (p.Arg243Gly)
c.529C>G (p.Arg177Gly)
n.799C>G
n.789C>G
 dbSNP
2g.47412495C>TCA040214MSH2c.727C>T (p.Arg243Trp)
c.529C>T (p.Arg177Trp)
n.799C>T
n.789C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.47412496G>ACA022108MSH2c.728G>A (p.Arg243Gln)
c.530G>A (p.Arg177Gln)
n.800G>A
n.790G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412496G>CCA346732181MSH2c.728G>C (p.Arg243Pro)
c.530G>C (p.Arg177Pro)
n.800G>C
n.790G>C
 ClinVar dbSNP
2g.47412496G=CA2495832739MSH2c.728G= (p.Arg243=)
c.530G= (p.Arg177=)
n.800G=
n.790G=
2g.47412496G>TCA346732184MSH2c.728G>T (p.Arg243Leu)
c.530G>T (p.Arg177Leu)
n.800G>T
n.790G>T
 gnomAD v4
2g.47412496_47412497delCA2580066904MSH2c.728_729del (p.Arg243LeufsTer12)
c.530_531del (p.Arg177LeufsTer12)
n.800_801del
n.790_791del
 ClinVar
2g.47412497dupCA658655710MSH2c.729dup (p.Leu244ValfsTer12)
c.531dup (p.Leu178ValfsTer12)
n.801dup
n.791dup
 ClinVar dbSNP
2g.47412497G>ACA425967752MSH2c.729G>A (p.Arg243=)
c.531G>A (p.Arg177=)
n.801G>A
n.791G>A
2g.47412497G>CCA425967753MSH2c.729G>C (p.Arg243=)
c.531G>C (p.Arg177=)
n.801G>C
n.791G>C
 dbSNP
2g.47412497G>TCA425967755MSH2c.729G>T (p.Arg243=)
c.531G>T (p.Arg177=)
n.801G>T
n.791G>T
 dbSNP
2g.47412497_47412498delinsGTCA2495832740MSH2c.729_730delinsGT (p.Arg243=)
c.531_532delinsGT (p.Arg177=)
n.801_802delinsGT
n.791_792delinsGT
2g.47412498T>ACA346732186MSH2c.730T>A (p.Leu244Met)
c.532T>A (p.Leu178Met)
n.802T>A
n.792T>A
 ClinVar dbSNP gnomAD v4
2g.47412498T>CCA425967757MSH2c.730T>C (p.Leu244=)
c.532T>C (p.Leu178=)
n.802T>C
n.792T>C
2g.47412498T>GCA346732189MSH2c.730T>G (p.Leu244Val)
c.532T>G (p.Leu178Val)
n.802T>G
n.792T>G
2g.47412499dupCA645531413MSH2c.731dup (p.Leu244PhefsTer12)
c.533dup (p.Leu178PhefsTer12)
n.803dup
n.793dup
 COSMIC
2g.47412499delCA10577947MSH2c.731del (p.Leu244CysfsTer2)
c.533del (p.Leu178CysfsTer2)
n.803del
n.793del
 ClinVar dbSNP
2g.47412499_47412502dupCA2695200766MSH2c.731_734dup (p.Leu245PhefsTer12)
c.533_536dup (p.Leu179PhefsTer12)
n.803_806dup
n.793_796dup
 ClinVar
2g.47412499T>ACA346732197MSH2c.731T>A (p.Leu244Ter)
c.533T>A (p.Leu178Ter)
n.803T>A
n.793T>A
 ClinVar dbSNP
2g.47412499T>CCA346732192MSH2c.731T>C (p.Leu244Ser)
c.533T>C (p.Leu178Ser)
n.803T>C
n.793T>C
 ClinVar dbSNP
2g.47412499T>GCA346732194MSH2c.731T>G (p.Leu244Trp)
c.533T>G (p.Leu178Trp)
n.803T>G
n.793T>G
 ClinVar
2g.47412499T=CA2495832741MSH2c.731T= (p.Leu244=)
c.533T= (p.Leu178=)
n.803T=
n.793T=
2g.47412499_47412503delCA2749801326MSH2c.731_735del (p.Leu244Ter)
c.533_537del (p.Leu178Ter)
n.803_807del
n.793_797del
2g.47412500delCA913187367MSH2c.732del (p.Leu244PhefsTer2)
c.534del (p.Leu178PhefsTer2)
n.804del
n.794del
2g.47412500G>ACA425967766MSH2c.732G>A (p.Leu244=)
c.534G>A (p.Leu178=)
n.804G>A
n.794G>A
 ClinVar dbSNP
2g.47412500G>CCA346732200MSH2c.732G>C (p.Leu244Phe)
c.534G>C (p.Leu178Phe)
n.804G>C
n.794G>C
 dbSNP
2g.47412500G>TCA346732201MSH2c.732G>T (p.Leu244Phe)
c.534G>T (p.Leu178Phe)
n.804G>T
n.794G>T
 ClinVar
2g.47412501T>ACA346732206MSH2c.733T>A (p.Leu245Met)
c.535T>A (p.Leu179Met)
n.805T>A
n.795T>A
 dbSNP
2g.47412501T>CCA425967771MSH2c.733T>C (p.Leu245=)
c.535T>C (p.Leu179=)
n.805T>C
n.795T>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47412501T>GCA346732208MSH2c.733T>G (p.Leu245Val)
c.535T>G (p.Leu179Val)
n.805T>G
n.795T>G
2g.47412501T=CA2495832742MSH2c.733T= (p.Leu245=)
c.535T= (p.Leu179=)
n.805T=
n.795T=
2g.47412502T>ACA346732213MSH2c.734T>A (p.Leu245Ter)
c.536T>A (p.Leu179Ter)
n.806T>A
n.796T>A
2g.47412502T>CCA346732215MSH2c.734T>C (p.Leu245Ser)
c.536T>C (p.Leu179Ser)
n.806T>C
n.796T>C
 ClinVar dbSNP
2g.47412502T>GCA346732217MSH2c.734T>G (p.Leu245Trp)
c.536T>G (p.Leu179Trp)
n.806T>G
n.796T>G
 ClinVar dbSNP
2g.47412502T=CA2495832743MSH2c.734T= (p.Leu245=)
c.536T= (p.Leu179=)
n.806T=
n.796T=
2g.47412503G>ACA425967780MSH2c.735G>A (p.Leu245=)
c.537G>A (p.Leu179=)
n.807G>A
n.797G>A
 ClinVar gnomAD v4
2g.47412503G>CCA348622MSH2c.735G>C (p.Leu245Phe)
c.537G>C (p.Leu179Phe)
n.807G>C
n.797G>C
 ClinVar dbSNP
2g.47412503G=CA2495832744MSH2c.735G= (p.Leu245=)
c.537G= (p.Leu179=)
n.807G=
n.797G=
2g.47412503G>TCA16617561MSH2c.735G>T (p.Leu245Phe)
c.537G>T (p.Leu179Phe)
n.807G>T
n.797G>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47412503dupCA022114MSH2c.735dup (p.Lys246GlufsTer10)
c.537dup (p.Lys180GlufsTer10)
n.807dup
n.797dup
 ClinVar dbSNP
2g.47412503_47412504insTGTTCA2586969198MSH2c.735_736insTGTT (p.Lys246CysfsTer2)
c.537_538insTGTT (p.Lys180CysfsTer2)
n.807_808insTGTT
n.797_798insTGTT
2g.47412504A=CA2495832745MSH2c.736A= (p.Lys246=)
c.538A= (p.Lys180=)
n.808A=
n.798A=
2g.47412504A>CCA022120MSH2c.736A>C (p.Lys246Gln)
c.538A>C (p.Lys180Gln)
n.808A>C
n.798A>C
 ClinVar dbSNP
2g.47412504A>GCA346732225MSH2c.736A>G (p.Lys246Glu)
c.538A>G (p.Lys180Glu)
n.808A>G
n.798A>G
 ClinVar dbSNP
2g.47412504A>TCA022126MSH2c.736A>T (p.Lys246Ter)
c.538A>T (p.Lys180Ter)
n.808A>T
n.798A>T
 ClinVar dbSNP
2g.47412506delCA2573051954MSH2c.738del (p.Gly247AlafsTer7)
c.540del (p.Gly181AlafsTer7)
n.810del
n.800del
 ClinVar dbSNP
2g.47412505A=CA2495832746MSH2c.737A= (p.Lys246=)
c.539A= (p.Lys180=)
n.809A=
n.799A=
2g.47412505A>CCA346732229MSH2c.737A>C (p.Lys246Thr)
c.539A>C (p.Lys180Thr)
n.809A>C
n.799A>C
2g.47412505A>GCA346732232MSH2c.737A>G (p.Lys246Arg)
c.539A>G (p.Lys180Arg)
n.809A>G
n.799A>G
 dbSNP
2g.47412505A>TCA346732235MSH2c.737A>T (p.Lys246Ile)
c.539A>T (p.Lys180Ile)
n.809A>T
n.799A>T
 dbSNP
2g.47412506A=CA2495832748MSH2c.738A= (p.Lys246=)
c.540A= (p.Lys180=)
n.810A=
n.800A=
2g.47412506A>CCA346732238MSH2c.738A>C (p.Lys246Asn)
c.540A>C (p.Lys180Asn)
n.810A>C
n.800A>C
 ClinVar dbSNP
2g.47412506A>GCA425967795MSH2c.738A>G (p.Lys246=)
c.540A>G (p.Lys180=)
n.810A>G
n.800A>G
 ClinVar dbSNP
2g.47412506A>TCA346732241MSH2c.738A>T (p.Lys246Asn)
c.540A>T (p.Lys180Asn)
n.810A>T
n.800A>T
 dbSNP
2g.47412506_47412509delinsAGGCCA2495832747MSH2c.738_741delinsAGGC (p.Lys246=)
c.540_543delinsAGGC (p.Lys180=)
n.810_813delinsAGGC
n.800_803delinsAGGC
2g.47412507G>ACA346732244MSH2c.739G>A (p.Gly247Ser)
c.541G>A (p.Gly181Ser)
n.811G>A
n.801G>A
2g.47412507G>CCA346732247MSH2c.739G>C (p.Gly247Arg)
c.541G>C (p.Gly181Arg)
n.811G>C
n.801G>C
 ClinVar dbSNP
2g.47412507G>TCA346732252MSH2c.739G>T (p.Gly247Cys)
c.541G>T (p.Gly181Cys)
n.811G>T
n.801G>T
2g.47412508dupCA2499214025MSH2c.740dup (p.Lys248GlnfsTer8)
c.542dup (p.Lys182GlnfsTer8)
n.812dup
n.802dup
2g.47412507_47412509delCA532705153MSH2c.739_741del (p.Gly247del)
c.541_543del (p.Gly181del)
n.811_813del
n.801_803del
 dbSNP gnomAD v2
2g.47412508G>ACA346732256MSH2c.740G>A (p.Gly247Asp)
c.542G>A (p.Gly181Asp)
n.812G>A
n.802G>A
 dbSNP
2g.47412508G>CCA346732258MSH2c.740G>C (p.Gly247Ala)
c.542G>C (p.Gly181Ala)
n.812G>C
n.802G>C
 dbSNP
2g.47412508G>TCA346732261MSH2c.740G>T (p.Gly247Val)
c.542G>T (p.Gly181Val)
n.812G>T
n.802G>T
2g.47412509C>ACA425967810MSH2c.741C>A (p.Gly247=)
c.543C>A (p.Gly181=)
n.813C>A
n.803C>A
 ClinVar dbSNP
2g.47412509C=CA2495832750MSH2c.741C= (p.Gly247=)
c.543C= (p.Gly181=)
n.813C=
n.803C=
2g.47412509C>GCA040241MSH2c.741C>G (p.Gly247=)
c.543C>G (p.Gly181=)
n.813C>G
n.803C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47412509C>TCA425967808MSH2c.741C>T (p.Gly247=)
c.543C>T (p.Gly181=)
n.813C>T
n.803C>T
 ClinVar dbSNP
2g.47412509_47412510delinsCACA2495832749MSH2c.741_742delinsCA (p.Gly247=)
c.543_544delinsCA (p.Gly181=)
n.813_814delinsCA
n.803_804delinsCA
2g.47412510A=CA2495832751MSH2c.742A= (p.Lys248=)
c.544A= (p.Lys182=)
n.814A=
n.804A=
2g.47412510A>CCA346732278MSH2c.742A>C (p.Lys248Gln)
c.544A>C (p.Lys182Gln)
n.814A>C
n.804A>C
 ClinVar dbSNP
2g.47412510A>GCA022149MSH2c.742A>G (p.Lys248Glu)
c.544A>G (p.Lys182Glu)
n.814A>G
n.804A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412510A>TCA346732275MSH2c.742A>T (p.Lys248Ter)
c.544A>T (p.Lys182Ter)
n.814A>T
n.804A>T
 ClinVar
2g.47412514_47412515insAAAAAAACA532705154MSH2c.746_747insAAAAAAA (p.Gly250LysfsTer8)
c.548_549insAAAAAAA (p.Gly184LysfsTer8)
n.818_819insAAAAAAA
n.808_809insAAAAAAA
 gnomAD v2
2g.47412514dupCA1139656925MSH2c.746dup (p.Glu251ArgfsTer5)
c.548dup (p.Glu185ArgfsTer5)
n.818dup
n.808dup
 ClinVar dbSNP
2g.47412514delCA022155MSH2c.746del (p.Lys249ArgfsTer5)
c.548del (p.Lys183ArgfsTer5)
n.818del
n.808del
 ClinVar dbSNP gnomAD v4
2g.47412511A=CA2495832752MSH2c.743A= (p.Lys248=)
c.545A= (p.Lys182=)
n.815A=
n.805A=
2g.47412511A>CCA346732281MSH2c.743A>C (p.Lys248Thr)
c.545A>C (p.Lys182Thr)
n.815A>C
n.805A>C
2g.47412511A>GCA16617562MSH2c.743A>G (p.Lys248Arg)
c.545A>G (p.Lys182Arg)
n.815A>G
n.805A>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47412511A>TCA346732285MSH2c.743A>T (p.Lys248Ile)
c.545A>T (p.Lys182Ile)
n.815A>T
n.805A>T
2g.47412512A=CA2495832753MSH2c.744A= (p.Lys248=)
c.546A= (p.Lys182=)
n.816A=
n.806A=
2g.47412512A>CCA16610847MSH2c.744A>C (p.Lys248Asn)
c.546A>C (p.Lys182Asn)
n.816A>C
n.806A>C
 ClinVar dbSNP gnomAD v4
2g.47412512A>GCA425967837MSH2c.744A>G (p.Lys248=)
c.546A>G (p.Lys182=)
n.816A>G
n.806A>G
2g.47412512A>TCA346732288MSH2c.744A>T (p.Lys248Asn)
c.546A>T (p.Lys182Asn)
n.816A>T
n.806A>T
 dbSNP
2g.47412513A>CCA346732290MSH2c.745A>C (p.Lys249Gln)
c.547A>C (p.Lys183Gln)
n.817A>C
n.807A>C
2g.47412513A>GCA346732292MSH2c.745A>G (p.Lys249Glu)
c.547A>G (p.Lys183Glu)
n.817A>G
n.807A>G
 ClinVar
2g.47412513A>TCA346732293MSH2c.745A>T (p.Lys249Ter)
c.547A>T (p.Lys183Ter)
n.817A>T
n.807A>T
2g.47412514A=CA2495832754MSH2c.746A= (p.Lys249=)
c.548A= (p.Lys183=)
n.818A=
n.808A=
2g.47412514A>CCA16617563MSH2c.746A>C (p.Lys249Thr)
c.548A>C (p.Lys183Thr)
n.818A>C
n.808A>C
 ClinVar dbSNP gnomAD v4
2g.47412514A>GCA346732298MSH2c.746A>G (p.Lys249Arg)
c.548A>G (p.Lys183Arg)
n.818A>G
n.808A>G
 ClinVar dbSNP
2g.47412514A>TCA346732301MSH2c.746A>T (p.Lys249Met)
c.548A>T (p.Lys183Met)
n.818A>T
n.808A>T
2g.47412514_47412515delCA2586969199MSH2c.746_747del (p.Lys249ArgfsTer6)
c.548_549del (p.Lys183ArgfsTer6)
n.818_819del
n.808_809del
 ClinVar gnomAD v4
2g.47412516_47412519delCA2695200772MSH2c.748_751del (p.Gly250SerfsTer3)
c.550_553del (p.Gly184SerfsTer3)
n.820_823del
n.810_813del
 ClinVar
2g.47412515_47412525delCA2699270010MSH2c.747_757del (p.Lys249AsnfsTer3)
c.549_559del (p.Lys183AsnfsTer3)
n.819_829del
n.809_819del
 dbSNP
2g.47412515G>ACA022163MSH2c.747G>A (p.Lys249=)
c.549G>A (p.Lys183=)
n.819G>A
n.809G>A
 ClinVar dbSNP
2g.47412515G>CCA10584209MSH2c.747G>C (p.Lys249Asn)
c.549G>C (p.Lys183Asn)
n.819G>C
n.809G>C
 ClinVar dbSNP
2g.47412515G=CA2495832755MSH2c.747G= (p.Lys249=)
c.549G= (p.Lys183=)
n.819G=
n.809G=
2g.47412515G>TCA346732305MSH2c.747G>T (p.Lys249Asn)
c.549G>T (p.Lys183Asn)
n.819G>T
n.809G>T
 dbSNP
2g.47412517delCA645531414MSH2c.749del (p.Gly250GlufsTer4)
c.551del (p.Gly184GlufsTer4)
n.821del
n.811del
 ClinVar COSMIC
2g.47412516G>ACA346732311MSH2c.748G>A (p.Gly250Arg)
c.550G>A (p.Gly184Arg)
n.820G>A
n.810G>A
 ClinVar dbSNP gnomAD v4
2g.47412516G>CCA346732314MSH2c.748G>C (p.Gly250Arg)
c.550G>C (p.Gly184Arg)
n.820G>C
n.810G>C
2g.47412516G=CA2495832756MSH2c.748G= (p.Gly250=)
c.550G= (p.Gly184=)
n.820G=
n.810G=
2g.47412516G>TCA348603MSH2c.748G>T (p.Gly250Ter)
c.550G>T (p.Gly184Ter)
n.820G>T
n.810G>T
 ClinVar dbSNP
2g.47412517G>ACA022167MSH2c.749G>A (p.Gly250Glu)
c.551G>A (p.Gly184Glu)
n.821G>A
n.811G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
2g.47412517G>CCA346732319MSH2c.749G>C (p.Gly250Ala)
c.551G>C (p.Gly184Ala)
n.821G>C
n.811G>C
2g.47412517G=CA2495832757MSH2c.749G= (p.Gly250=)
c.551G= (p.Gly184=)
n.821G=
n.811G=
2g.47412517G>TCA022174MSH2c.749G>T (p.Gly250Val)
c.551G>T (p.Gly184Val)
n.821G>T
n.811G>T
 ClinVar dbSNP
2g.47412518A>CCA425967867MSH2c.750A>C (p.Gly250=)
c.552A>C (p.Gly184=)
n.822A>C
n.812A>C
2g.47412518A>GCA425967869MSH2c.750A>G (p.Gly250=)
c.552A>G (p.Gly184=)
n.822A>G
n.812A>G
 ClinVar dbSNP
2g.47412518A>TCA425967871MSH2c.750A>T (p.Gly250=)
c.552A>T (p.Gly184=)
n.822A>T
n.812A>T
2g.47412519G>ACA040269MSH2c.751G>A (p.Glu251Lys)
c.553G>A (p.Glu185Lys)
n.823G>A
n.813G>A
 ClinVar dbSNP ExAC gnomAD v4
2g.47412519G>CCA346732322MSH2c.751G>C (p.Glu251Gln)
c.553G>C (p.Glu185Gln)
n.823G>C
n.813G>C
 dbSNP
2g.47412519G=CA2495832758MSH2c.751G= (p.Glu251=)
c.553G= (p.Glu185=)
n.823G=
n.813G=
2g.47412519G>TCA346732324MSH2c.751G>T (p.Glu251Ter)
c.553G>T (p.Glu185Ter)
n.823G>T
n.813G>T
2g.47412520A>CCA346732327MSH2c.752A>C (p.Glu251Ala)
c.554A>C (p.Glu185Ala)
n.824A>C
n.814A>C
2g.47412520A>GCA346732328MSH2c.752A>G (p.Glu251Gly)
c.554A>G (p.Glu185Gly)
n.824A>G
n.814A>G
 ClinVar dbSNP
2g.47412520A>TCA346732330MSH2c.752A>T (p.Glu251Val)
c.554A>T (p.Glu185Val)
n.824A>T
n.814A>T
 dbSNP
2g.47412521G>ACA425967882MSH2c.753G>A (p.Glu251=)
c.555G>A (p.Glu185=)
n.825G>A
n.815G>A
 ClinVar dbSNP
2g.47412521G>CCA346732332MSH2c.753G>C (p.Glu251Asp)
c.555G>C (p.Glu185Asp)
n.825G>C
n.815G>C
2g.47412521G=CA2495832759MSH2c.753G= (p.Glu251=)
c.555G= (p.Glu185=)
n.825G=
n.815G=
2g.47412521G>TCA346732334MSH2c.753G>T (p.Glu251Asp)
c.555G>T (p.Glu185Asp)
n.825G>T
n.815G>T
2g.47412522C>ACA346732342MSH2c.754C>A (p.Gln252Lys)
c.556C>A (p.Gln186Lys)
n.826C>A
n.816C>A
 dbSNP
2g.47412522C=CA2495832760MSH2c.754C= (p.Gln252=)
c.556C= (p.Gln186=)
n.826C=
n.816C=
2g.47412522C>GCA46681506MSH2c.754C>G (p.Gln252Glu)
c.556C>G (p.Gln186Glu)
n.826C>G
n.816C>G
 dbSNP
2g.47412522C>TCA022185MSH2c.754C>T (p.Gln252Ter)
c.556C>T (p.Gln186Ter)
n.826C>T
n.816C>T
 ClinVar dbSNP gnomAD v4
2g.47412523A=CA2495832761MSH2c.755A= (p.Gln252=)
c.557A= (p.Gln186=)
n.827A=
n.817A=
2g.47412523A>CCA10577948MSH2c.755A>C (p.Gln252Pro)
c.557A>C (p.Gln186Pro)
n.827A>C
n.817A>C
 ClinVar dbSNP gnomAD v4
2g.47412523A>GCA040278MSH2c.755A>G (p.Gln252Arg)
c.557A>G (p.Gln186Arg)
n.827A>G
n.817A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412523A>TCA346732348MSH2c.755A>T (p.Gln252Leu)
c.557A>T (p.Gln186Leu)
n.827A>T
n.817A>T
 ClinVar
2g.47412523_47412526dupCA2573134699MSH2c.755_758dup (p.Met253IlefsTer4)
c.557_560dup (p.Met187IlefsTer4)
n.827_830dup
n.817_820dup
 ClinVar dbSNP
2g.47412524G>ACA425967900MSH2c.756G>A (p.Gln252=)
c.558G>A (p.Gln186=)
n.828G>A
n.818G>A
 dbSNP
2g.47412524G>CCA040292MSH2c.756G>C (p.Gln252His)
c.558G>C (p.Gln186His)
n.828G>C
n.818G>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47412524G=CA2495832762MSH2c.756G= (p.Gln252=)
c.558G= (p.Gln186=)
n.828G=
n.818G=
2g.47412524G>TCA346732351MSH2c.756G>T (p.Gln252His)
c.558G>T (p.Gln186His)
n.828G>T
n.818G>T
 ClinVar dbSNP
2g.47412524_47412528delinsGATGACA2495832763MSH2c.756_760delinsGATGA (p.Gln252=)
c.558_562delinsGATGA (p.Gln186=)
n.828_832delinsGATGA
n.818_822delinsGATGA
2g.47412524_47412525insCCA46681529MSH2c.756_757insC (p.Met253HisfsTer3)
c.558_559insC (p.Met187HisfsTer3)
n.828_829insC
n.818_819insC
 dbSNP
2g.47412525A=CA2495832764MSH2c.757A= (p.Met253=)
c.559A= (p.Met187=)
n.829A=
n.819A=
2g.47412525A>CCA346732354MSH2c.757A>C (p.Met253Leu)
c.559A>C (p.Met187Leu)
n.829A>C
n.819A>C
2g.47412525A>GCA346732357MSH2c.757A>G (p.Met253Val)
c.559A>G (p.Met187Val)
n.829A>G
n.819A>G
 ClinVar dbSNP gnomAD v4
2g.47412525A>TCA346732359MSH2c.757A>T (p.Met253Leu)
c.559A>T (p.Met187Leu)
n.829A>T
n.819A>T
 ClinVar dbSNP
2g.47412527_47412530delCA022190MSH2c.759_762del (p.Met253IlefsTer20)
c.561_564del (p.Met187IlefsTer20)
n.831_834del
n.821_824del
 ClinVar dbSNP
2g.47412526T>ACA346732361MSH2c.758T>A (p.Met253Lys)
c.560T>A (p.Met187Lys)
n.830T>A
n.820T>A
 dbSNP
2g.47412526T>CCA346732363MSH2c.758T>C (p.Met253Thr)
c.560T>C (p.Met187Thr)
n.830T>C
n.820T>C
 ClinVar dbSNP
2g.47412526T>GCA346732365MSH2c.758T>G (p.Met253Arg)
c.560T>G (p.Met187Arg)
n.830T>G
n.820T>G
 ClinVar dbSNP
2g.47412526dupCA2695200773MSH2c.758dup (p.Met253IlefsTer3)
c.560dup (p.Met187IlefsTer3)
n.830dup
n.820dup
 ClinVar
2g.47412526_47412527delinsTGCA2495832765MSH2c.758_759delinsTG (p.Met253=)
c.560_561delinsTG (p.Met187=)
n.830_831delinsTG
n.820_821delinsTG
2g.47412527delCA022195MSH2c.759del (p.Met253IlefsTer21)
c.561del (p.Met187IlefsTer21)
n.831del
n.821del
 ClinVar dbSNP
2g.47412527G>ACA16610795MSH2c.759G>A (p.Met253Ile)
c.561G>A (p.Met187Ile)
n.831G>A
n.821G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47412527G>CCA346732367MSH2c.759G>C (p.Met253Ile)
c.561G>C (p.Met187Ile)
n.831G>C
n.821G>C
 ClinVar dbSNP
2g.47412527G=CA2495832767MSH2c.759G= (p.Met253=)
c.561G= (p.Met187=)
n.831G=
n.821G=
2g.47412527G>TCA346732369MSH2c.759G>T (p.Met253Ile)
c.561G>T (p.Met187Ile)
n.831G>T
n.821G>T
 dbSNP
2g.47412527_47412528delinsGACA2495832766MSH2c.759_760delinsGA (p.Met253=)
c.561_562delinsGA (p.Met187=)
n.831_832delinsGA
n.821_822delinsGA
2g.47412530_47412548delCA2573051955MSH2c.762_780del (p.Asn254LysfsTer14)
c.564_582del (p.Asn188LysfsTer14)
n.834_852del
n.824_842del
 ClinVar dbSNP
2g.47412528A>CCA346732372MSH2c.760A>C (p.Asn254His)
c.562A>C (p.Asn188His)
n.832A>C
n.822A>C
 ClinVar
2g.47412528A>GCA346732373MSH2c.760A>G (p.Asn254Asp)
c.562A>G (p.Asn188Asp)
n.832A>G
n.822A>G
 ClinVar dbSNP
2g.47412528A>TCA346732376MSH2c.760A>T (p.Asn254Tyr)
c.562A>T (p.Asn188Tyr)
n.832A>T
n.822A>T
 dbSNP
2g.47412529dupCA2580066923MSH2c.761dup (p.Asn254LysfsTer2)
c.563dup (p.Asn188LysfsTer2)
n.833dup
n.823dup
 ClinVar
2g.47412529delCA022201MSH2c.761del (p.Asn254IlefsTer20)
c.563del (p.Asn188IlefsTer20)
n.833del
n.823del
 ClinVar dbSNP
2g.47412529A=CA2495832768MSH2c.761A= (p.Asn254=)
c.563A= (p.Asn188=)
n.833A=
n.823A=
2g.47412529A>CCA346732380MSH2c.761A>C (p.Asn254Thr)
c.563A>C (p.Asn188Thr)
n.833A>C
n.823A>C
 ClinVar
2g.47412529A>GCA346732382MSH2c.761A>G (p.Asn254Ser)
c.563A>G (p.Asn188Ser)
n.833A>G
n.823A>G
 ClinVar dbSNP gnomAD v4
2g.47412529A>TCA346732384MSH2c.761A>T (p.Asn254Ile)
c.563A>T (p.Asn188Ile)
n.833A>T
n.823A>T
2g.47412530_47412531delCA2695200777MSH2c.762_763del (p.Asn254LysfsTer29)
c.564_565del (p.Asn188LysfsTer29)
n.834_835del
n.824_825del
 ClinVar
2g.47412530T>ACA346732386MSH2c.762T>A (p.Asn254Lys)
c.564T>A (p.Asn188Lys)
n.834T>A
n.824T>A
 dbSNP
2g.47412530T>CCA022206MSH2c.762T>C (p.Asn254=)
c.564T>C (p.Asn188=)
n.834T>C
n.824T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412530T>GCA346732390MSH2c.762T>G (p.Asn254Lys)
c.564T>G (p.Asn188Lys)
n.834T>G
n.824T>G
2g.47412530T=CA2495832770MSH2c.762T= (p.Asn254=)
c.564T= (p.Asn188=)
n.834T=
n.824T=
2g.47412530dupCA2695200778MSH2c.762dup (p.Ser255Ter)
c.564dup (p.Ser189Ter)
n.834dup
n.824dup
 ClinVar
2g.47412530_47412534delinsTAGTGCA2495832769MSH2c.762_766delinsTAGTG (p.Asn254=)
c.564_568delinsTAGTG (p.Asn188=)
n.834_838delinsTAGTG
n.824_828delinsTAGTG
2g.47412531delCA2580066928MSH2c.763del (p.Ser255ValfsTer19)
c.565del (p.Ser189ValfsTer19)
n.835del
n.825del
 ClinVar
2g.47412531A=CA2495832771MSH2c.763A= (p.Ser255=)
c.565A= (p.Ser189=)
n.835A=
n.825A=
2g.47412531A>CCA346732397MSH2c.763A>C (p.Ser255Arg)
c.565A>C (p.Ser189Arg)
n.835A>C
n.825A>C
 ClinVar dbSNP gnomAD v2
2g.47412531A>GCA040330MSH2c.763A>G (p.Ser255Gly)
c.565A>G (p.Ser189Gly)
n.835A>G
n.825A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412531A>TCA346732394MSH2c.763A>T (p.Ser255Cys)
c.565A>T (p.Ser189Cys)
n.835A>T
n.825A>T
2g.47412531_47412534delinsTTCA022212MSH2c.763_766delinsTT (p.Ser255PhefsTer28)
c.565_568delinsTT (p.Ser189PhefsTer28)
n.835_838delinsTT
n.825_828delinsTT
 ClinVar dbSNP
2g.47412532G>ACA040340MSH2c.764G>A (p.Ser255Asn)
c.566G>A (p.Ser189Asn)
n.836G>A
n.826G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47412532G>CCA46681579MSH2c.764G>C (p.Ser255Thr)
c.566G>C (p.Ser189Thr)
n.836G>C
n.826G>C
 ClinVar dbSNP gnomAD v4
2g.47412532G=CA2495832772MSH2c.764G= (p.Ser255=)
c.566G= (p.Ser189=)
n.836G=
n.826G=
2g.47412532G>TCA346732401MSH2c.764G>T (p.Ser255Ile)
c.566G>T (p.Ser189Ile)
n.836G>T
n.826G>T
2g.47412532_47412544delCA2580066930MSH2c.764_776del (p.Ser255LysfsTer15)
c.566_578del (p.Ser189LysfsTer15)
n.836_848del
n.826_838del
 ClinVar
2g.47412533T>ACA346732404MSH2c.765T>A (p.Ser255Arg)
c.567T>A (p.Ser189Arg)
n.837T>A
n.827T>A
 dbSNP
2g.47412533T>CCA46681580MSH2c.765T>C (p.Ser255=)
c.567T>C (p.Ser189=)
n.837T>C
n.827T>C
 ClinVar dbSNP
2g.47412533T>GCA346732405MSH2c.765T>G (p.Ser255Arg)
c.567T>G (p.Ser189Arg)
n.837T>G
n.827T>G
2g.47412533T=CA2495832773MSH2c.765T= (p.Ser255=)
c.567T= (p.Ser189=)
n.837T=
n.827T=
2g.47412533dupCA2580066931MSH2c.765dup (p.Ala256CysfsTer28)
c.567dup (p.Ala190CysfsTer28)
n.837dup
n.827dup
 ClinVar
2g.47412534G>ACA022219MSH2c.766G>A (p.Ala256Thr)
c.568G>A (p.Ala190Thr)
n.838G>A
n.828G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412534G>CCA346732409MSH2c.766G>C (p.Ala256Pro)
c.568G>C (p.Ala190Pro)
n.838G>C
n.828G>C
 dbSNP
2g.47412534G=CA2495832774MSH2c.766G= (p.Ala256=)
c.568G= (p.Ala190=)
n.838G=
n.828G=
2g.47412534G>TCA346732411MSH2c.766G>T (p.Ala256Ser)
c.568G>T (p.Ala190Ser)
n.838G>T
n.828G>T
 dbSNP
2g.47412535C>ACA346732413MSH2c.767C>A (p.Ala256Asp)
c.569C>A (p.Ala190Asp)
n.839C>A
n.829C>A
2g.47412535C=CA2495832775MSH2c.767C= (p.Ala256=)
c.569C= (p.Ala190=)
n.839C=
n.829C=
2g.47412535C>GCA346732414MSH2c.767C>G (p.Ala256Gly)
c.569C>G (p.Ala190Gly)
n.839C>G
n.829C>G
 dbSNP gnomAD v2 gnomAD v4
2g.47412535C>TCA346732415MSH2c.767C>T (p.Ala256Val)
c.569C>T (p.Ala190Val)
n.839C>T
n.829C>T
 ClinVar dbSNP gnomAD v4
2g.47412535_47412536dupCA331679MSH2c.767_768dup (p.Val257LeufsTer18)
c.569_570dup (p.Val191LeufsTer18)
n.839_840dup
n.829_830dup
 ClinVar dbSNP
2g.47412536T>ACA425967964MSH2c.768T>A (p.Ala256=)
c.570T>A (p.Ala190=)
n.840T>A
n.830T>A
2g.47412536T>CCA46681592MSH2c.768T>C (p.Ala256=)
c.570T>C (p.Ala190=)
n.840T>C
n.830T>C
 ClinVar dbSNP gnomAD v4
2g.47412536T>GCA425967967MSH2c.768T>G (p.Ala256=)
c.570T>G (p.Ala190=)
n.840T>G
n.830T>G
2g.47412536T=CA2495832776MSH2c.768T= (p.Ala256=)
c.570T= (p.Ala190=)
n.840T=
n.830T=
2g.47412537G>ACA10577949MSH2c.769G>A (p.Val257Ile)
c.571G>A (p.Val191Ile)
n.841G>A
n.831G>A
 ClinVar dbSNP
2g.47412537G>CCA346732421MSH2c.769G>C (p.Val257Leu)
c.571G>C (p.Val191Leu)
n.841G>C
n.831G>C
 dbSNP
2g.47412537G=CA2495832777MSH2c.769G= (p.Val257=)
c.571G= (p.Val191=)
n.841G=
n.831G=
2g.47412537G>TCA346732419MSH2c.769G>T (p.Val257Leu)
c.571G>T (p.Val191Leu)
n.841G>T
n.831G>T
 ClinVar
2g.47412537_47412539delinsGTACA2495832778MSH2c.769_771delinsGTA (p.Val257=)
c.571_573delinsGTA (p.Val191=)
n.841_843delinsGTA
n.831_833delinsGTA
2g.47412538_47412554delCA2580066932MSH2c.770_786del (p.Val257GlufsTer21)
c.572_588del (p.Val191GlufsTer21)
n.842_858del
n.832_848del
 ClinVar
2g.47412538T>ACA346732423MSH2c.770T>A (p.Val257Glu)
c.572T>A (p.Val191Glu)
n.842T>A
n.832T>A
 dbSNP
2g.47412538T>CCA346732428MSH2c.770T>C (p.Val257Ala)
c.572T>C (p.Val191Ala)
n.842T>C
n.832T>C
 ClinVar
2g.47412538T>GCA346732426MSH2c.770T>G (p.Val257Gly)
c.572T>G (p.Val191Gly)
n.842T>G
n.832T>G
2g.47412539_47412540delCA913187987MSH2c.771_772del (p.Leu258AlafsTer25)
c.573_574del (p.Leu192AlafsTer25)
n.843_844del
n.833_834del
 ClinVar dbSNP
2g.47412539A=CA2495832779MSH2c.771A= (p.Val257=)
c.573A= (p.Val191=)
n.843A=
n.833A=
2g.47412539A>CCA425967973MSH2c.771A>C (p.Val257=)
c.573A>C (p.Val191=)
n.843A>C
n.833A>C
 ClinVar dbSNP
2g.47412539A>GCA425967975MSH2c.771A>G (p.Val257=)
c.573A>G (p.Val191=)
n.843A>G
n.833A>G
 ClinVar
2g.47412539A>TCA425967976MSH2c.771A>T (p.Val257=)
c.573A>T (p.Val191=)
n.843A>T
n.833A>T
 ClinVar dbSNP gnomAD v4
2g.47412540T>ACA346732430MSH2c.772T>A (p.Leu258Met)
c.574T>A (p.Leu192Met)
n.844T>A
n.834T>A
2g.47412540T>CCA425967981MSH2c.772T>C (p.Leu258=)
c.574T>C (p.Leu192=)
n.844T>C
n.834T>C
2g.47412540T>GCA346732432MSH2c.772T>G (p.Leu258Val)
c.574T>G (p.Leu192Val)
n.844T>G
n.834T>G
2g.47412540_47412541insCCA2658946233MSH2c.772_773insC (p.Leu258SerfsTer26)
c.574_575insC (p.Leu192SerfsTer26)
n.844_845insC
n.834_835insC
 gnomAD v4
2g.47412541T>ACA346732434MSH2c.773T>A (p.Leu258Ter)
c.575T>A (p.Leu192Ter)
n.845T>A
n.835T>A
 ClinVar dbSNP
2g.47412541T>CCA346732436MSH2c.773T>C (p.Leu258Ser)
c.575T>C (p.Leu192Ser)
n.845T>C
n.835T>C
2g.47412541T>GCA346732438MSH2c.773T>G (p.Leu258Trp)
c.575T>G (p.Leu192Trp)
n.845T>G
n.835T>G
2g.47412542G>ACA040381MSH2c.774G>A (p.Leu258=)
c.576G>A (p.Leu192=)
n.846G>A
n.836G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412542G>CCA346732443MSH2c.774G>C (p.Leu258Phe)
c.576G>C (p.Leu192Phe)
n.846G>C
n.836G>C
2g.47412542G=CA2495832780MSH2c.774G= (p.Leu258=)
c.576G= (p.Leu192=)
n.846G=
n.836G=
2g.47412542G>TCA040395MSH2c.774G>T (p.Leu258Phe)
c.576G>T (p.Leu192Phe)
n.846G>T
n.836G>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47412543C>ACA346732446MSH2c.775C>A (p.Pro259Thr)
c.577C>A (p.Pro193Thr)
n.847C>A
n.837C>A
 dbSNP gnomAD v4
2g.47412543C=CA2495832781MSH2c.775C= (p.Pro259=)
c.577C= (p.Pro193=)
n.847C=
n.837C=
2g.47412543C>GCA346732447MSH2c.775C>G (p.Pro259Ala)
c.577C>G (p.Pro193Ala)
n.847C>G
n.837C>G
 dbSNP
2g.47412543C>TCA022230MSH2c.775C>T (p.Pro259Ser)
c.577C>T (p.Pro193Ser)
n.847C>T
n.837C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47412544delCA2586969206MSH2c.776del (p.Pro259GlnfsTer15)
c.578del (p.Pro193GlnfsTer15)
n.848del
n.838del
 ClinVar
2g.47412544C>ACA46681638MSH2c.776C>A (p.Pro259Gln)
c.578C>A (p.Pro193Gln)
n.848C>A
n.838C>A
 dbSNP
2g.47412544C=CA2495832782MSH2c.776C= (p.Pro259=)
c.578C= (p.Pro193=)
n.848C=
n.838C=
2g.47412544C>GCA346732452MSH2c.776C>G (p.Pro259Arg)
c.578C>G (p.Pro193Arg)
n.848C>G
n.838C>G
 ClinVar dbSNP
2g.47412544C>TCA346732454MSH2c.776C>T (p.Pro259Leu)
c.578C>T (p.Pro193Leu)
n.848C>T
n.838C>T
 ClinVar dbSNP
2g.47412545A=CA2495832783MSH2c.777A= (p.Pro259=)
c.579A= (p.Pro193=)
n.849A=
n.839A=
2g.47412545A>CCA425968004MSH2c.777A>C (p.Pro259=)
c.579A>C (p.Pro193=)
n.849A>C
n.839A>C
2g.47412545A>GCA46681641MSH2c.777A>G (p.Pro259=)
c.579A>G (p.Pro193=)
n.849A>G
n.839A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
2g.47412545A>TCA425968009MSH2c.777A>T (p.Pro259=)
c.579A>T (p.Pro193=)
n.849A>T
n.839A>T
 ClinVar dbSNP

Number of alleles fetched