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.47414262_47414868delinsATTTTAGGTTGCAGTTTCATCACTGTCTGCGGTAATCAAGTTTTTAGAACTCTTATCAGATGATTCCAACTTTGGACAGTTTGAACTGACTACTTTTGACTTCAGCCAGTATATGAAATTGGATATTGCAGCAGTCAGAGCCCTTAACCTTTTTCAGGTAAAAAAAAAAAAAAAAAAAAAAAAAAAGGGTTAAAAATGTTGAATGGTTAAAAAATGTTTTCATTGACATATACTGAAGAAGCTTATAAAGGAGCTAAAATATTTTGAAATATTATTATACTTGGATTAGATAACTAGCTTTAAATGGCTGTATTTTTCTCTCCCCTCCTCCACTCCACTTTTTAACTTTTTTTTTTTTAAGTCAGAGTCTCACTTGTTCCCTAGGCCAGAGTGCAGTGGCACAATCTCAGCCCACTCTAACCTCCACCTCCCAAGTAGTTGGGATTACAGTTGCCTGCCACCATGCCTGGTTAATTTTTATATTTTTAGTAGGGTTGCGGGGACAGGGTTTCACCATGTTGGCCAGGTTGGTCTCAAACTTCTGACCTTAGGTGATCCTCCCACCTCGGCTTCCCAAAGTGCTGGGATTACAGGCTTGAGCCATCGTCA2495833736MSH2c.793-7_942+450delinsATTTTAGGTTGCAGTTTCATCACTGTCTGCGGTAATCAAGTTTTTAGAACTCTTATCAGATGATTCCAACTTTGGACAGTTTGAACTGACTACTTTTGACTTCAGCCAGTATATGAAATTGGATATTGCAGCAGTCAGAGCCCTTAACCTTTTTCAGGTAAAAAAAAAAAAAAAAAAAAAAAAAAAGGGTTAAAAATGTTGAATGGTTAAAAAATGTTTTCATTGACATATACTGAAGAAGCTTATAAAGGAGCTAAAATATTTTGAAATATTATTATACTTGGATTAGATAACTAGCTTTAAATGGCTGTATTTTTCTCTCCCCTCCTCCACTCCACTTTTTAACTTTTTTTTTTTTAAGTCAGAGTCTCACTTGTTCCCTAGGCCAGAGTGCAGTGGCACAATCTCAGCCCACTCTAACCTCCACCTCCCAAGTAGTTGGGATTACAGTTGCCTGCCACCATGCCTGGTTAATTTTTATATTTTTAGTAGGGTTGCGGGGACAGGGTTTCACCATGTTGGCCAGGTTGGTCTCAAACTTCTGACCTTAGGTGATCCTCCCACCTCGGCTTCCCAAAGTGCTGGGATTACAGGCTTGAGCCATCGT
c.595-7_744+450delinsATTTTAGGTTGCAGTTTCATCACTGTCTGCGGTAATCAAGTTTTTAGAACTCTTATCAGATGATTCCAACTTTGGACAGTTTGAACTGACTACTTTTGACTTCAGCCAGTATATGAAATTGGATATTGCAGCAGTCAGAGCCCTTAACCTTTTTCAGGTAAAAAAAAAAAAAAAAAAAAAAAAAAAGGGTTAAAAATGTTGAATGGTTAAAAAATGTTTTCATTGACATATACTGAAGAAGCTTATAAAGGAGCTAAAATATTTTGAAATATTATTATACTTGGATTAGATAACTAGCTTTAAATGGCTGTATTTTTCTCTCCCCTCCTCCACTCCACTTTTTAACTTTTTTTTTTTTAAGTCAGAGTCTCACTTGTTCCCTAGGCCAGAGTGCAGTGGCACAATCTCAGCCCACTCTAACCTCCACCTCCCAAGTAGTTGGGATTACAGTTGCCTGCCACCATGCCTGGTTAATTTTTATATTTTTAGTAGGGTTGCGGGGACAGGGTTTCACCATGTTGGCCAGGTTGGTCTCAAACTTCTGACCTTAGGTGATCCTCCCACCTCGGCTTCCCAAAGTGCTGGGATTACAGGCTTGAGCCATCGT
n.865-7_1014+450delinsATTTTAGGTTGCAGTTTCATCACTGTCTGCGGTAATCAAGTTTTTAGAACTCTTATCAGATGATTCCAACTTTGGACAGTTTGAACTGACTACTTTTGACTTCAGCCAGTATATGAAATTGGATATTGCAGCAGTCAGAGCCCTTAACCTTTTTCAGGTAAAAAAAAAAAAAAAAAAAAAAAAAAAGGGTTAAAAATGTTGAATGGTTAAAAAATGTTTTCATTGACATATACTGAAGAAGCTTATAAAGGAGCTAAAATATTTTGAAATATTATTATACTTGGATTAGATAACTAGCTTTAAATGGCTGTATTTTTCTCTCCCCTCCTCCACTCCACTTTTTAACTTTTTTTTTTTTAAGTCAGAGTCTCACTTGTTCCCTAGGCCAGAGTGCAGTGGCACAATCTCAGCCCACTCTAACCTCCACCTCCCAAGTAGTTGGGATTACAGTTGCCTGCCACCATGCCTGGTTAATTTTTATATTTTTAGTAGGGTTGCGGGGACAGGGTTTCACCATGTTGGCCAGGTTGGTCTCAAACTTCTGACCTTAGGTGATCCTCCCACCTCGGCTTCCCAAAGTGCTGGGATTACAGGCTTGAGCCATCGT
n.855-7_1004+450delinsATTTTAGGTTGCAGTTTCATCACTGTCTGCGGTAATCAAGTTTTTAGAACTCTTATCAGATGATTCCAACTTTGGACAGTTTGAACTGACTACTTTTGACTTCAGCCAGTATATGAAATTGGATATTGCAGCAGTCAGAGCCCTTAACCTTTTTCAGGTAAAAAAAAAAAAAAAAAAAAAAAAAAAGGGTTAAAAATGTTGAATGGTTAAAAAATGTTTTCATTGACATATACTGAAGAAGCTTATAAAGGAGCTAAAATATTTTGAAATATTATTATACTTGGATTAGATAACTAGCTTTAAATGGCTGTATTTTTCTCTCCCCTCCTCCACTCCACTTTTTAACTTTTTTTTTTTTAAGTCAGAGTCTCACTTGTTCCCTAGGCCAGAGTGCAGTGGCACAATCTCAGCCCACTCTAACCTCCACCTCCCAAGTAGTTGGGATTACAGTTGCCTGCCACCATGCCTGGTTAATTTTTATATTTTTAGTAGGGTTGCGGGGACAGGGTTTCACCATGTTGGCCAGGTTGGTCTCAAACTTCTGACCTTAGGTGATCCTCCCACCTCGGCTTCCCAAAGTGCTGGGATTACAGGCTTGAGCCATCGT
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.47414267_47416282delCA2499216016MSH2c.793-2_943-14del
c.595-2_745-14del
n.865-2_1015-14del
n.855-2_1005-14del
 ClinVar
2g.47414278_47414315delCA2580066985MSH2c.802_839del (p.Ser268IlefsTer3)
c.604_641del (p.Ser202IlefsTer3)
n.874_911del
n.864_901del
 ClinVar
2g.47414306delCA2499216018MSH2c.830del (p.Leu277Ter)
c.632del (p.Leu211Ter)
n.902del
n.892del
 ClinVar dbSNP
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
 ClinVar
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
2g.47414362T>ACA346732910MSH2c.886T>A (p.Phe296Ile)
c.688T>A (p.Phe230Ile)
n.958T>A
n.948T>A
2g.47414362T>CCA346732911MSH2c.886T>C (p.Phe296Leu)
c.688T>C (p.Phe230Leu)
n.958T>C
n.948T>C
 ClinVar dbSNP
2g.47414362T>GCA346732912MSH2c.886T>G (p.Phe296Val)
c.688T>G (p.Phe230Val)
n.958T>G
n.948T>G
2g.47414363delCA913189183MSH2c.887del (p.Phe296SerfsTer5)
c.689del (p.Phe230SerfsTer5)
n.959del
n.949del
 ClinVar
2g.47414362_47414367delinsTTCAGCCA2495834001MSH2c.886_891delinsTTCAGC (p.Phe296=)
c.688_693delinsTTCAGC (p.Phe230=)
n.958_963delinsTTCAGC
n.948_953delinsTTCAGC
2g.47414363T>ACA346732913MSH2c.887T>A (p.Phe296Tyr)
c.689T>A (p.Phe230Tyr)
n.959T>A
n.949T>A
 ClinVar dbSNP gnomAD v4
2g.47414363T>CCA346732914MSH2c.887T>C (p.Phe296Ser)
c.689T>C (p.Phe230Ser)
n.959T>C
n.949T>C
 ClinVar dbSNP
2g.47414363T>GCA346732915MSH2c.887T>G (p.Phe296Cys)
c.689T>G (p.Phe230Cys)
n.959T>G
n.949T>G
 ClinVar
2g.47414363T=CA2495834003MSH2c.887T= (p.Phe296=)
c.689T= (p.Phe230=)
n.959T=
n.949T=
2g.47414363_47414364delinsTCCA2495834002MSH2c.887_888delinsTC (p.Phe296=)
c.689_690delinsTC (p.Phe230=)
n.959_960delinsTC
n.949_950delinsTC
2g.47414363_47414367delinsACTTTTTCAGTATATGACTACTTTTGACTACTTTTTCA915943892MSH2c.887_891delinsACTTTTTCAGTATATGACTACTTTTGACTACTTTTT (p.Phe296TyrfsTer6)
c.689_693delinsACTTTTTCAGTATATGACTACTTTTGACTACTTTTT (p.Phe230TyrfsTer6)
n.959_963delinsACTTTTTCAGTATATGACTACTTTTGACTACTTTTT
n.949_953delinsACTTTTTCAGTATATGACTACTTTTGACTACTTTTT
 ClinVar dbSNP
2g.47414364delCA022475MSH2c.888del (p.Phe296LeufsTer5)
c.690del (p.Phe230LeufsTer5)
n.960del
n.950del
 ClinVar dbSNP
2g.47414364C>ACA346732916MSH2c.888C>A (p.Phe296Leu)
c.690C>A (p.Phe230Leu)
n.960C>A
n.950C>A
 dbSNP
2g.47414364C=CA2495834004MSH2c.888C= (p.Phe296=)
c.690C= (p.Phe230=)
n.960C=
n.950C=
2g.47414364C>GCA10577958MSH2c.888C>G (p.Phe296Leu)
c.690C>G (p.Phe230Leu)
n.960C>G
n.950C>G
 ClinVar dbSNP gnomAD v4
2g.47414364C>TCA425970107MSH2c.888C>T (p.Phe296=)
c.690C>T (p.Phe230=)
n.960C>T
n.950C>T
 ClinVar dbSNP gnomAD v4
2g.47414365A=CA2495834005MSH2c.889A= (p.Ser297=)
c.691A= (p.Ser231=)
n.961A=
n.951A=
2g.47414365A>CCA346732917MSH2c.889A>C (p.Ser297Arg)
c.691A>C (p.Ser231Arg)
n.961A>C
n.951A>C
2g.47414365A>GCA346732918MSH2c.889A>G (p.Ser297Gly)
c.691A>G (p.Ser231Gly)
n.961A>G
n.951A>G
 ClinVar dbSNP
2g.47414365A>TCA346732919MSH2c.889A>T (p.Ser297Cys)
c.691A>T (p.Ser231Cys)
n.961A>T
n.951A>T
 dbSNP
2g.47414366G>ACA346732920MSH2c.890G>A (p.Ser297Asn)
c.692G>A (p.Ser231Asn)
n.962G>A
n.952G>A
 ClinVar dbSNP
2g.47414366G>CCA346732921MSH2c.890G>C (p.Ser297Thr)
c.692G>C (p.Ser231Thr)
n.962G>C
n.952G>C
2g.47414366G=CA2495834006MSH2c.890G= (p.Ser297=)
c.692G= (p.Ser231=)
n.962G=
n.952G=
2g.47414366G>TCA346732922MSH2c.890G>T (p.Ser297Ile)
c.692G>T (p.Ser231Ile)
n.962G>T
n.952G>T
 gnomAD v4
2g.47414367C>ACA346732923MSH2c.891C>A (p.Ser297Arg)
c.693C>A (p.Ser231Arg)
n.963C>A
n.953C>A
 dbSNP
2g.47414367C=CA2495834007MSH2c.891C= (p.Ser297=)
c.693C= (p.Ser231=)
n.963C=
n.953C=
2g.47414367C>GCA10584210MSH2c.891C>G (p.Ser297Arg)
c.693C>G (p.Ser231Arg)
n.963C>G
n.953C>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.47414367C>TCA425970121MSH2c.891C>T (p.Ser297=)
c.693C>T (p.Ser231=)
n.963C>T
n.953C>T
 ClinVar dbSNP
2g.47414368C>ACA346732924MSH2c.892C>A (p.Gln298Lys)
c.694C>A (p.Gln232Lys)
n.964C>A
n.954C>A
 dbSNP
2g.47414368C=CA2495834008MSH2c.892C= (p.Gln298=)
c.694C= (p.Gln232=)
n.964C=
n.954C=
2g.47414368C>GCA346732925MSH2c.892C>G (p.Gln298Glu)
c.694C>G (p.Gln232Glu)
n.964C>G
n.954C>G
 dbSNP
2g.47414368C>TCA022486MSH2c.892C>T (p.Gln298Ter)
c.694C>T (p.Gln232Ter)
n.964C>T
n.954C>T
 ClinVar dbSNP gnomAD v4
2g.47414369A=CA2495834009MSH2c.893A= (p.Gln298=)
c.695A= (p.Gln232=)
n.965A=
n.955A=
2g.47414369A>CCA46684157MSH2c.893A>C (p.Gln298Pro)
c.695A>C (p.Gln232Pro)
n.965A>C
n.955A>C
 dbSNP
2g.47414369A>GCA346732927MSH2c.893A>G (p.Gln298Arg)
c.695A>G (p.Gln232Arg)
n.965A>G
n.955A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47414369A>TCA346732926MSH2c.893A>T (p.Gln298Leu)
c.695A>T (p.Gln232Leu)
n.965A>T
n.955A>T
 dbSNP
2g.47414370G>ACA425970137MSH2c.894G>A (p.Gln298=)
c.696G>A (p.Gln232=)
n.966G>A
n.956G>A
 ClinVar dbSNP
2g.47414370G>CCA022491MSH2c.894G>C (p.Gln298His)
c.696G>C (p.Gln232His)
n.966G>C
n.956G>C
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.47414370G=CA2495834010MSH2c.894G= (p.Gln298=)
c.696G= (p.Gln232=)
n.966G=
n.956G=
2g.47414370G>TCA346732928MSH2c.894G>T (p.Gln298His)
c.696G>T (p.Gln232His)
n.966G>T
n.956G>T
 ClinVar
2g.47414371T>ACA346732929MSH2c.895T>A (p.Tyr299Asn)
c.697T>A (p.Tyr233Asn)
n.967T>A
n.957T>A
 ClinVar dbSNP
2g.47414371T>CCA346732930MSH2c.895T>C (p.Tyr299His)
c.697T>C (p.Tyr233His)
n.967T>C
n.957T>C
 ClinVar dbSNP COSMIC
2g.47414371T>GCA346732931MSH2c.895T>G (p.Tyr299Asp)
c.697T>G (p.Tyr233Asp)
n.967T>G
n.957T>G
 dbSNP
2g.47414374_47414375dupCA022502MSH2c.898_899dup (p.Met300IlefsTer2)
c.700_701dup (p.Met234IlefsTer2)
n.970_971dup
n.960_961dup
 ClinVar dbSNP
2g.47414372A=CA2495834011MSH2c.896A= (p.Tyr299=)
c.698A= (p.Tyr233=)
n.968A=
n.958A=
2g.47414372A>CCA346732934MSH2c.896A>C (p.Tyr299Ser)
c.698A>C (p.Tyr233Ser)
n.968A>C
n.958A>C
2g.47414372A>GCA346732933MSH2c.896A>G (p.Tyr299Cys)
c.698A>G (p.Tyr233Cys)
n.968A>G
n.958A>G
 ClinVar dbSNP gnomAD v4
2g.47414372A>TCA346732932MSH2c.896A>T (p.Tyr299Phe)
c.698A>T (p.Tyr233Phe)
n.968A>T
n.958A>T
 dbSNP
2g.47414373T>ACA346732935MSH2c.897T>A (p.Tyr299Ter)
c.699T>A (p.Tyr233Ter)
n.969T>A
n.959T>A
 ClinVar dbSNP
2g.47414373T>CCA425970155MSH2c.897T>C (p.Tyr299=)
c.699T>C (p.Tyr233=)
n.969T>C
n.959T>C
 ClinVar dbSNP gnomAD v4
2g.47414373T>GCA10584211MSH2c.897T>G (p.Tyr299Ter)
c.699T>G (p.Tyr233Ter)
n.969T>G
n.959T>G
 ClinVar dbSNP
2g.47414373T=CA2495834012MSH2c.897T= (p.Tyr299=)
c.699T= (p.Tyr233=)
n.969T=
n.959T=
2g.47414374A=CA2495834013MSH2c.898A= (p.Met300=)
c.700A= (p.Met234=)
n.970A=
n.960A=
2g.47414374A>CCA346732936MSH2c.898A>C (p.Met300Leu)
c.700A>C (p.Met234Leu)
n.970A>C
n.960A>C
2g.47414374A>GCA022496MSH2c.898A>G (p.Met300Val)
c.700A>G (p.Met234Val)
n.970A>G
n.960A>G
 ClinVar dbSNP
2g.47414374A>TCA346732937MSH2c.898A>T (p.Met300Leu)
c.700A>T (p.Met234Leu)
n.970A>T
n.960A>T
 dbSNP
2g.47414375T>ACA346732938MSH2c.899T>A (p.Met300Lys)
c.701T>A (p.Met234Lys)
n.971T>A
n.961T>A
 dbSNP
2g.47414375T>CCA346732940MSH2c.899T>C (p.Met300Thr)
c.701T>C (p.Met234Thr)
n.971T>C
n.961T>C
 dbSNP
2g.47414375T>GCA346732939MSH2c.899T>G (p.Met300Arg)
c.701T>G (p.Met234Arg)
n.971T>G
n.961T>G
2g.47414376G>ACA022513MSH2c.900G>A (p.Met300Ile)
c.702G>A (p.Met234Ile)
n.972G>A
n.962G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.47414376G>CCA346732941MSH2c.900G>C (p.Met300Ile)
c.702G>C (p.Met234Ile)
n.972G>C
n.962G>C
 dbSNP
2g.47414376G=CA2495834014MSH2c.900G= (p.Met300=)
c.702G= (p.Met234=)
n.972G=
n.962G=
2g.47414376G>TCA346732942MSH2c.900G>T (p.Met300Ile)
c.702G>T (p.Met234Ile)
n.972G>T
n.962G>T
 ClinVar dbSNP
2g.47414377A=CA2495834015MSH2c.901A= (p.Lys301=)
c.703A= (p.Lys235=)
n.973A=
n.963A=
2g.47414377A>CCA346732943MSH2c.901A>C (p.Lys301Gln)
c.703A>C (p.Lys235Gln)
n.973A>C
n.963A>C
 ClinVar
2g.47414377A>GCA346732944MSH2c.901A>G (p.Lys301Glu)
c.703A>G (p.Lys235Glu)
n.973A>G
n.963A>G
2g.47414377A>TCA022518MSH2c.901A>T (p.Lys301Ter)
c.703A>T (p.Lys235Ter)
n.973A>T
n.963A>T
 ClinVar dbSNP
2g.47414378A>CCA346732945MSH2c.902A>C (p.Lys301Thr)
c.704A>C (p.Lys235Thr)
n.974A>C
n.964A>C
2g.47414378A>GCA346732946MSH2c.902A>G (p.Lys301Arg)
c.704A>G (p.Lys235Arg)
n.974A>G
n.964A>G
 ClinVar
2g.47414378A>TCA346732947MSH2c.902A>T (p.Lys301Ile)
c.704A>T (p.Lys235Ile)
n.974A>T
n.964A>T
 dbSNP
2g.47414379A>CCA346732948MSH2c.903A>C (p.Lys301Asn)
c.705A>C (p.Lys235Asn)
n.975A>C
n.965A>C
2g.47414379A>GCA425970192MSH2c.903A>G (p.Lys301=)
c.705A>G (p.Lys235=)
n.975A>G
n.965A>G
 gnomAD v4
2g.47414379A>TCA346732949MSH2c.903A>T (p.Lys301Asn)
c.705A>T (p.Lys235Asn)
n.975A>T
n.965A>T
 dbSNP
2g.47414380T>ACA346732951MSH2c.904T>A (p.Leu302Met)
c.706T>A (p.Leu236Met)
n.976T>A
n.966T>A
 ClinVar dbSNP gnomAD v4
2g.47414380T>CCA10577959MSH2c.904T>C (p.Leu302=)
c.706T>C (p.Leu236=)
n.976T>C
n.966T>C
 ClinVar dbSNP
2g.47414380T>GCA346732950MSH2c.904T>G (p.Leu302Val)
c.706T>G (p.Leu236Val)
n.976T>G
n.966T>G
2g.47414380T=CA2495834016MSH2c.904T= (p.Leu302=)
c.706T= (p.Leu236=)
n.976T=
n.966T=
2g.47414381T>ACA022523MSH2c.905T>A (p.Leu302Ter)
c.707T>A (p.Leu236Ter)
n.977T>A
n.967T>A
 ClinVar dbSNP
2g.47414381T>CCA10577960MSH2c.905T>C (p.Leu302Ser)
c.707T>C (p.Leu236Ser)
n.977T>C
n.967T>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47414381T>GCA346732952MSH2c.905T>G (p.Leu302Trp)
c.707T>G (p.Leu236Trp)
n.977T>G
n.967T>G
 gnomAD v4
2g.47414381T=CA2495834017MSH2c.905T= (p.Leu302=)
c.707T= (p.Leu236=)
n.977T=
n.967T=
2g.47414382G>ACA022528MSH2c.906G>A (p.Leu302=)
c.708G>A (p.Leu236=)
n.978G>A
n.968G>A
 ClinVar dbSNP
2g.47414382G>CCA346732953MSH2c.906G>C (p.Leu302Phe)
c.708G>C (p.Leu236Phe)
n.978G>C
n.968G>C
 ClinVar dbSNP
2g.47414382G=CA2495834018MSH2c.906G= (p.Leu302=)
c.708G= (p.Leu236=)
n.978G=
n.968G=
2g.47414382G>TCA346732954MSH2c.906G>T (p.Leu302Phe)
c.708G>T (p.Leu236Phe)
n.978G>T
n.968G>T
2g.47414383G>ACA16617568MSH2c.907G>A (p.Asp303Asn)
c.709G>A (p.Asp237Asn)
n.979G>A
n.969G>A
 ClinVar dbSNP
2g.47414383G>CCA346732955MSH2c.907G>C (p.Asp303His)
c.709G>C (p.Asp237His)
n.979G>C
n.969G>C
 ClinVar dbSNP
2g.47414383G=CA2495834019MSH2c.907G= (p.Asp303=)
c.709G= (p.Asp237=)
n.979G=
n.969G=
2g.47414383G>TCA346732956MSH2c.907G>T (p.Asp303Tyr)
c.709G>T (p.Asp237Tyr)
n.979G>T
n.969G>T
 dbSNP
2g.47414384delCA2580067061MSH2c.908del (p.Asp303ValfsTer28)
c.710del (p.Asp237ValfsTer28)
n.980del
n.970del
 ClinVar
2g.47414384A>CCA346732957MSH2c.908A>C (p.Asp303Ala)
c.710A>C (p.Asp237Ala)
n.980A>C
n.970A>C
2g.47414384A>GCA346732958MSH2c.908A>G (p.Asp303Gly)
c.710A>G (p.Asp237Gly)
n.980A>G
n.970A>G
 ClinVar dbSNP gnomAD v4
2g.47414384A>TCA346732959MSH2c.908A>T (p.Asp303Val)
c.710A>T (p.Asp237Val)
n.980A>T
n.970A>T
 ClinVar dbSNP
2g.47414385T>ACA346732960MSH2c.909T>A (p.Asp303Glu)
c.711T>A (p.Asp237Glu)
n.981T>A
n.971T>A
 dbSNP gnomAD v3 gnomAD v4
2g.47414385T>CCA425970222MSH2c.909T>C (p.Asp303=)
c.711T>C (p.Asp237=)
n.981T>C
n.971T>C
 ClinVar
2g.47414385T>GCA346732961MSH2c.909T>G (p.Asp303Glu)
c.711T>G (p.Asp237Glu)
n.981T>G
n.971T>G
 dbSNP
2g.47414386A=CA2495834020MSH2c.910A= (p.Ile304=)
c.712A= (p.Ile238=)
n.982A=
n.972A=
2g.47414386A>CCA346732964MSH2c.910A>C (p.Ile304Leu)
c.712A>C (p.Ile238Leu)
n.982A>C
n.972A>C
 dbSNP
2g.47414386A>GCA346732962MSH2c.910A>G (p.Ile304Val)
c.712A>G (p.Ile238Val)
n.982A>G
n.972A>G
 ClinVar dbSNP
2g.47414386A>TCA346732963MSH2c.910A>T (p.Ile304Phe)
c.712A>T (p.Ile238Phe)
n.982A>T
n.972A>T
 ClinVar dbSNP
2g.47414387T>ACA346732965MSH2c.911T>A (p.Ile304Asn)
c.713T>A (p.Ile238Asn)
n.983T>A
n.973T>A
 dbSNP
2g.47414387T>CCA46684227MSH2c.911T>C (p.Ile304Thr)
c.713T>C (p.Ile238Thr)
n.983T>C
n.973T>C
 ClinVar dbSNP gnomAD v4
2g.47414387T>GCA346732966MSH2c.911T>G (p.Ile304Ser)
c.713T>G (p.Ile238Ser)
n.983T>G
n.973T>G
2g.47414387T=CA2495834021MSH2c.911T= (p.Ile304=)
c.713T= (p.Ile238=)
n.983T=
n.973T=
2g.47414388dupCA337334MSH2c.912dup (p.Ala305CysfsTer7)
c.714dup (p.Ala239CysfsTer7)
n.984dup
n.974dup
 ClinVar dbSNP
2g.47414388T>ACA425970243MSH2c.912T>A (p.Ile304=)
c.714T>A (p.Ile238=)
n.984T>A
n.974T>A
2g.47414388T>CCA022533MSH2c.912T>C (p.Ile304=)
c.714T>C (p.Ile238=)
n.984T>C
n.974T>C
 ClinVar dbSNP
2g.47414388T>GCA346732967MSH2c.912T>G (p.Ile304Met)
c.714T>G (p.Ile238Met)
n.984T>G
n.974T>G
2g.47414388T=CA2495834022MSH2c.912T= (p.Ile304=)
c.714T= (p.Ile238=)
n.984T=
n.974T=
2g.47414388_47414398delinsTGCAGCAGTCACA2495834023MSH2c.912_922delinsTGCAGCAGTCA (p.Ile304=)
c.714_724delinsTGCAGCAGTCA (p.Ile238=)
n.984_994delinsTGCAGCAGTCA
n.974_984delinsTGCAGCAGTCA
2g.47414389G>ACA022539MSH2c.913G>A (p.Ala305Thr)
c.715G>A (p.Ala239Thr)
n.985G>A
n.975G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47414389G>CCA346732968MSH2c.913G>C (p.Ala305Pro)
c.715G>C (p.Ala239Pro)
n.985G>C
n.975G>C
 dbSNP
2g.47414389G=CA2495834024MSH2c.913G= (p.Ala305=)
c.715G= (p.Ala239=)
n.985G=
n.975G=
2g.47414389G>TCA346732969MSH2c.913G>T (p.Ala305Ser)
c.715G>T (p.Ala239Ser)
n.985G>T
n.975G>T
 dbSNP
2g.47414389dupCA197206MSH2c.913dup (p.Ala305GlyfsTer7)
c.715dup (p.Ala239GlyfsTer7)
n.985dup
n.975dup
 ClinVar dbSNP
2g.47414390_47414399delCA658760380MSH2c.914_923del (p.Ala305GlufsTer23)
c.716_725del (p.Ala239GlufsTer23)
n.986_995del
n.976_985del
 ClinVar dbSNP
2g.47414390C>ACA041105MSH2c.914C>A (p.Ala305Glu)
c.716C>A (p.Ala239Glu)
n.986C>A
n.976C>A
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.47414390C=CA2495834026MSH2c.914C= (p.Ala305=)
c.716C= (p.Ala239=)
n.986C=
n.976C=
2g.47414390C>GCA346732970MSH2c.914C>G (p.Ala305Gly)
c.716C>G (p.Ala239Gly)
n.986C>G
n.976C>G
 dbSNP gnomAD v4
2g.47414390C>TCA346732971MSH2c.914C>T (p.Ala305Val)
c.716C>T (p.Ala239Val)
n.986C>T
n.976C>T
 ClinVar dbSNP
2g.47414390_47414391delinsCACA2495834025MSH2c.914_915delinsCA (p.Ala305=)
c.716_717delinsCA (p.Ala239=)
n.986_987delinsCA
n.976_977delinsCA
2g.47414391delCA1139656935MSH2c.915del (p.Ala306GlnfsTer25)
c.717del (p.Ala240GlnfsTer25)
n.987del
n.977del
 ClinVar dbSNP
2g.47414391A=CA2495834027MSH2c.915A= (p.Ala305=)
c.717A= (p.Ala239=)
n.987A=
n.977A=
2g.47414391A>CCA041122MSH2c.915A>C (p.Ala305=)
c.717A>C (p.Ala239=)
n.987A>C
n.977A>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47414391A>GCA425970261MSH2c.915A>G (p.Ala305=)
c.717A>G (p.Ala239=)
n.987A>G
n.977A>G
 ClinVar dbSNP gnomAD v4
2g.47414391A>TCA425970259MSH2c.915A>T (p.Ala305=)
c.717A>T (p.Ala239=)
n.987A>T
n.977A>T
 dbSNP
2g.47414391_47414398dupCA022544MSH2c.915_922dup (p.Arg308LysfsTer26)
c.717_724dup (p.Arg242LysfsTer26)
n.987_994dup
n.977_984dup
 ClinVar dbSNP
2g.47414392G>ACA346732974MSH2c.916G>A (p.Ala306Thr)
c.718G>A (p.Ala240Thr)
n.988G>A
n.978G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47414392G>CCA346732972MSH2c.916G>C (p.Ala306Pro)
c.718G>C (p.Ala240Pro)
n.988G>C
n.978G>C
 dbSNP
2g.47414392G>TCA346732973MSH2c.916G>T (p.Ala306Ser)
c.718G>T (p.Ala240Ser)
n.988G>T
n.978G>T
 dbSNP
2g.47414392_47414393delinsATCA2573134973MSH2c.916_917delinsAT (p.Ala306Ile)
c.718_719delinsAT (p.Ala240Ile)
n.988_989delinsAT
n.978_979delinsAT
 ClinVar dbSNP
2g.47414393C>ACA346732975MSH2c.917C>A (p.Ala306Glu)
c.719C>A (p.Ala240Glu)
n.989C>A
n.979C>A
 dbSNP gnomAD v4
2g.47414393C=CA2495834028MSH2c.917C= (p.Ala306=)
c.719C= (p.Ala240=)
n.989C=
n.979C=
2g.47414393C>GCA346732976MSH2c.917C>G (p.Ala306Gly)
c.719C>G (p.Ala240Gly)
n.989C>G
n.979C>G
 ClinVar dbSNP gnomAD v4
2g.47414393C>TCA346732977MSH2c.917C>T (p.Ala306Val)
c.719C>T (p.Ala240Val)
n.989C>T
n.979C>T
 ClinVar dbSNP gnomAD v4
2g.47414393_47414394delCA2580067064MSH2c.917_918del (p.Ala306GlyfsTer5)
c.719_720del (p.Ala240GlyfsTer5)
n.989_990del
n.979_980del
 ClinVar
2g.47414396_47414399delCA2573134974MSH2c.920_923del (p.Val307GlufsTer23)
c.722_725del (p.Val241GlufsTer23)
n.992_995del
n.982_985del
 ClinVar dbSNP
2g.47414394A>CCA425970276MSH2c.918A>C (p.Ala306=)
c.720A>C (p.Ala240=)
n.990A>C
n.980A>C
 ClinVar dbSNP
2g.47414394A>GCA425970277MSH2c.918A>G (p.Ala306=)
c.720A>G (p.Ala240=)
n.990A>G
n.980A>G
 ClinVar dbSNP gnomAD v4
2g.47414394A>TCA425970279MSH2c.918A>T (p.Ala306=)
c.720A>T (p.Ala240=)
n.990A>T
n.980A>T
 dbSNP
2g.47414394_47414395delinsTTCA2573134975MSH2c.918_919delinsTT (p.Val307Phe)
c.720_721delinsTT (p.Val241Phe)
n.990_991delinsTT
n.980_981delinsTT
 ClinVar dbSNP
2g.47414395G>ACA346732978MSH2c.919G>A (p.Val307Ile)
c.721G>A (p.Val241Ile)
n.991G>A
n.981G>A
 dbSNP
2g.47414395G>CCA346732979MSH2c.919G>C (p.Val307Leu)
c.721G>C (p.Val241Leu)
n.991G>C
n.981G>C
 ClinVar dbSNP
2g.47414395G=CA2495834029MSH2c.919G= (p.Val307=)
c.721G= (p.Val241=)
n.991G=
n.981G=
2g.47414395G>TCA346732980MSH2c.919G>T (p.Val307Phe)
c.721G>T (p.Val241Phe)
n.991G>T
n.981G>T
 ClinVar dbSNP
2g.47414396T>ACA346732981MSH2c.920T>A (p.Val307Asp)
c.722T>A (p.Val241Asp)
n.992T>A
n.982T>A
 dbSNP
2g.47414396T>CCA346732982MSH2c.920T>C (p.Val307Ala)
c.722T>C (p.Val241Ala)
n.992T>C
n.982T>C
 dbSNP
2g.47414396T>GCA346732983MSH2c.920T>G (p.Val307Gly)
c.722T>G (p.Val241Gly)
n.992T>G
n.982T>G
 dbSNP
2g.47414397C>ACA425970292MSH2c.921C>A (p.Val307=)
c.723C>A (p.Val241=)
n.993C>A
n.983C>A
 dbSNP gnomAD v3 gnomAD v4
2g.47414397C=CA2495834030MSH2c.921C= (p.Val307=)
c.723C= (p.Val241=)
n.993C=
n.983C=
2g.47414397C>GCA425970293MSH2c.921C>G (p.Val307=)
c.723C>G (p.Val241=)
n.993C>G
n.983C>G
 ClinVar dbSNP
2g.47414397C>TCA425970295MSH2c.921C>T (p.Val307=)
c.723C>T (p.Val241=)
n.993C>T
n.983C>T
 ClinVar dbSNP
2g.47414397dupCA2573134976MSH2c.921dup (p.Arg308GlnfsTer4)
c.723dup (p.Arg242GlnfsTer4)
n.993dup
n.983dup
 ClinVar dbSNP
2g.47414398_47414402delCA2740097805MSH2c.922_926del (p.Arg308ProfsTer2)
c.724_728del (p.Arg242ProfsTer2)
n.994_998del
n.984_988del
 ClinVar
2g.47414398A>CCA425970300MSH2c.922A>C (p.Arg308=)
c.724A>C (p.Arg242=)
n.994A>C
n.984A>C
2g.47414398A>GCA346732984MSH2c.922A>G (p.Arg308Gly)
c.724A>G (p.Arg242Gly)
n.994A>G
n.984A>G
 ClinVar dbSNP
2g.47414398A>TCA346732985MSH2c.922A>T (p.Arg308Ter)
c.724A>T (p.Arg242Ter)
n.994A>T
n.984A>T
 dbSNP
2g.47414398dupCA2695200782MSH2c.922dup (p.Arg308LysfsTer4)
c.724dup (p.Arg242LysfsTer4)
n.994dup
n.984dup
 ClinVar
2g.47414400_47414401dupCA2580611364MSH2c.924_925dup (p.Ala309GlufsTer23)
c.726_727dup (p.Ala243GlufsTer23)
n.996_997dup
n.986_987dup
 ClinVar
2g.47414398_47414401dupCA2580611363MSH2c.922_925dup (p.Ala309GlufsTer4)
c.724_727dup (p.Ala243GlufsTer4)
n.994_997dup
n.984_987dup
 ClinVar
2g.47414400_47414401delCA2580611365MSH2c.924_925del (p.Arg308SerfsTer3)
c.726_727del (p.Arg242SerfsTer3)
n.996_997del
n.986_987del
 ClinVar
2g.47414399G>ACA346732986MSH2c.923G>A (p.Arg308Lys)
c.725G>A (p.Arg242Lys)
n.995G>A
n.985G>A
 ClinVar dbSNP
2g.47414399G>CCA346732987MSH2c.923G>C (p.Arg308Thr)
c.725G>C (p.Arg242Thr)
n.995G>C
n.985G>C
 ClinVar dbSNP gnomAD v4
2g.47414399G=CA2495834031MSH2c.923G= (p.Arg308=)
c.725G= (p.Arg242=)
n.995G=
n.985G=
2g.47414399G>TCA346732988MSH2c.923G>T (p.Arg308Ile)
c.725G>T (p.Arg242Ile)
n.995G>T
n.985G>T
 dbSNP gnomAD v4
2g.47414400A>CCA346732989MSH2c.924A>C (p.Arg308Ser)
c.726A>C (p.Arg242Ser)
n.996A>C
n.986A>C
2g.47414400A>GCA425970309MSH2c.924A>G (p.Arg308=)
c.726A>G (p.Arg242=)
n.996A>G
n.986A>G
 dbSNP
2g.47414400A>TCA346732990MSH2c.924A>T (p.Arg308Ser)
c.726A>T (p.Arg242Ser)
n.996A>T
n.986A>T
 dbSNP
2g.47414401G>ACA041137MSH2c.925G>A (p.Ala309Thr)
c.727G>A (p.Ala243Thr)
n.997G>A
n.987G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.47414401G>CCA346732991MSH2c.925G>C (p.Ala309Pro)
c.727G>C (p.Ala243Pro)
n.997G>C
n.987G>C
 ClinVar dbSNP
2g.47414401G=CA2495834033MSH2c.925G= (p.Ala309=)
c.727G= (p.Ala243=)
n.997G=
n.987G=
2g.47414401G>TCA346732992MSH2c.925G>T (p.Ala309Ser)
c.727G>T (p.Ala243Ser)
n.997G>T
n.987G>T
 ClinVar
2g.47414401_47414402delinsGCCA2495834032MSH2c.925_926delinsGC (p.Ala309=)
c.727_728delinsGC (p.Ala243=)
n.997_998delinsGC
n.987_988delinsGC
2g.47414402C>ACA346732993MSH2c.926C>A (p.Ala309Asp)
c.728C>A (p.Ala243Asp)
n.998C>A
n.988C>A
 dbSNP gnomAD v4
2g.47414402C=CA2495834034MSH2c.926C= (p.Ala309=)
c.728C= (p.Ala243=)
n.998C=
n.988C=
2g.47414402C>GCA346732994MSH2c.926C>G (p.Ala309Gly)
c.728C>G (p.Ala243Gly)
n.998C>G
n.988C>G
 dbSNP
2g.47414402C>TCA346732995MSH2c.926C>T (p.Ala309Val)
c.728C>T (p.Ala243Val)
n.998C>T
n.988C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47414404dupCA2739274423MSH2c.928dup (p.Leu310ProfsTer2)
c.730dup (p.Leu244ProfsTer2)
n.1000dup
n.990dup
 ClinVar
2g.47414404delCA16617569MSH2c.928del (p.Asn311ThrfsTer20)
c.730del (p.Asn245ThrfsTer20)
n.1000del
n.990del
 ClinVar dbSNP
2g.47414404_47414410delCA2580067066MSH2c.928_934del (p.Leu310PhefsTer19)
c.730_736del (p.Leu244PhefsTer19)
n.1000_1006del
n.990_996del
 ClinVar
2g.47414403C>ACA425970324MSH2c.927C>A (p.Ala309=)
c.729C>A (p.Ala243=)
n.999C>A
n.989C>A
 ClinVar dbSNP
2g.47414403C>GCA425970327MSH2c.927C>G (p.Ala309=)
c.729C>G (p.Ala243=)
n.999C>G
n.989C>G
 ClinVar dbSNP
2g.47414403C>TCA425970325MSH2c.927C>T (p.Ala309=)
c.729C>T (p.Ala243=)
n.999C>T
n.989C>T
 ClinVar dbSNP
2g.47414404C>ACA346732996MSH2c.928C>A (p.Leu310Ile)
c.730C>A (p.Leu244Ile)
n.1000C>A
n.990C>A
 gnomAD v4
2g.47414404C=CA2495834035MSH2c.928C= (p.Leu310=)
c.730C= (p.Leu244=)
n.1000C=
n.990C=
2g.47414404C>GCA041152MSH2c.928C>G (p.Leu310Val)
c.730C>G (p.Leu244Val)
n.1000C>G
n.990C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.47414404C>TCA346732997MSH2c.928C>T (p.Leu310Phe)
c.730C>T (p.Leu244Phe)
n.1000C>T
n.990C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.47414405T>ACA346732998MSH2c.929T>A (p.Leu310His)
c.731T>A (p.Leu244His)
n.1001T>A
n.991T>A
 dbSNP gnomAD v4
2g.47414405T>CCA022549MSH2c.929T>C (p.Leu310Pro)
c.731T>C (p.Leu244Pro)
n.1001T>C
n.991T>C
 ClinVar dbSNP
2g.47414405T>GCA022554MSH2c.929T>G (p.Leu310Arg)
c.731T>G (p.Leu244Arg)
n.1001T>G
n.991T>G
 ClinVar dbSNP
2g.47414405T=CA2495834036MSH2c.929T= (p.Leu310=)
c.731T= (p.Leu244=)
n.1001T=
n.991T=
2g.47414406delCA2580067071MSH2c.930del (p.Asn311ThrfsTer20)
c.732del (p.Asn245ThrfsTer20)
n.1002del
n.992del
 ClinVar

Number of alleles fetched