Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47345814_47346367delCA2580084293MYBPC3c.933_1090+396del
c.915_1072+396del
ClinVar
11g.47346242_47346313delinsAGCCTCTTTAGCATGCCGCGCAGGTCAGTGACGCCGTACTGGAAGGCGATGCGCTCGTACTCAGATGGGGGTCA1969339501MYBPC3c.984_1055delinsACCCCCATCTGAGTACGAGCGCATCGCCTTCCAGTACGGCGTCACTGACCTGCGCGGCATGCTAAAGAGGCT (p.Ala328=)
c.966_1037delinsACCCCCATCTGAGTACGAGCGCATCGCCTTCCAGTACGGCGTCACTGACCTGCGCGGCATGCTAAAGAGGCT (p.Ala322=)
11g.47346247_47346317delCA016227MYBPC3c.984_1054del (p.Pro329GlnfsTer7)
c.966_1036del (p.Pro323GlnfsTer7)
ClinVar dbSNP
11g.47346292G>ACA474220910MYBPC3c.1005C>T (p.Arg335=)
c.987C>T (p.Arg329=)
11g.47346292G>CCA474220908MYBPC3c.1005C>G (p.Arg335=)
c.987C>G (p.Arg329=)
11g.47346292G>TCA474220909MYBPC3c.1005C>A (p.Arg335=)
c.987C>A (p.Arg329=)
11g.47346293C>ACA380331454MYBPC3c.1004G>T (p.Arg335Leu)
c.986G>T (p.Arg329Leu)
gnomAD v4
11g.47346293C>GCA380331458MYBPC3c.1004G>C (p.Arg335Pro)
c.986G>C (p.Arg329Pro)
11g.47346293C>TCA380331459MYBPC3c.1004G>A (p.Arg335His)
c.986G>A (p.Arg329His)
gnomAD v4
11g.47346294G>ACA009677MYBPC3c.1003C>T (p.Arg335Cys)
c.985C>T (p.Arg329Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.47346294G>CCA380331461MYBPC3c.1003C>G (p.Arg335Gly)
c.985C>G (p.Arg329Gly)
11g.47346294G=CA1969339623MYBPC3c.1003C= (p.Arg335=)
c.985C= (p.Arg329=)
11g.47346294G>TCA380331460MYBPC3c.1003C>A (p.Arg335Ser)
c.985C>A (p.Arg329Ser)
dbSNP gnomAD v2 gnomAD v4
11g.47346295C>ACA380331463MYBPC3c.1002G>T (p.Glu334Asp)
c.984G>T (p.Glu328Asp)
11g.47346295C>GCA380331466MYBPC3c.1002G>C (p.Glu334Asp)
c.984G>C (p.Glu328Asp)
11g.47346295C>TCA474220913MYBPC3c.1002G>A (p.Glu334=)
c.984G>A (p.Glu328=)
gnomAD v4 COSMIC COSMIC
11g.47346296T>ACA380331470MYBPC3c.1001A>T (p.Glu334Val)
c.983A>T (p.Glu328Val)
11g.47346296T>CCA380331473MYBPC3c.1001A>G (p.Glu334Gly)
c.983A>G (p.Glu328Gly)
11g.47346296T>GCA380331479MYBPC3c.1001A>C (p.Glu334Ala)
c.983A>C (p.Glu328Ala)
11g.47346297C>ACA009672MYBPC3c.1000G>T (p.Glu334Ter)
c.982G>T (p.Glu328Ter)
ClinVar dbSNP gnomAD v4
11g.47346297C=CA1969339628MYBPC3c.1000G= (p.Glu334=)
c.982G= (p.Glu328=)
11g.47346297C>GCA380331485MYBPC3c.1000G>C (p.Glu334Gln)
c.982G>C (p.Glu328Gln)
11g.47346297C>TCA009667MYBPC3c.1000G>A (p.Glu334Lys)
c.982G>A (p.Glu328Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.47346298delCA2697548549MYBPC3c.999del (p.Tyr333Ter)
c.981del (p.Tyr327Ter)
ClinVar
11g.47346298G>ACA057719MYBPC3c.999C>T (p.Tyr333=)
c.981C>T (p.Tyr327=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47346298G>CCA016252MYBPC3c.999C>G (p.Tyr333Ter)
c.981C>G (p.Tyr327Ter)
ClinVar dbSNP
11g.47346298G=CA1969339631MYBPC3c.999C= (p.Tyr333=)
c.981C= (p.Tyr327=)
11g.47346298G>TCA380331492MYBPC3c.999C>A (p.Tyr333Ter)
c.981C>A (p.Tyr327Ter)
ClinVar dbSNP
11g.47346299T>ACA380331496MYBPC3c.998A>T (p.Tyr333Phe)
c.980A>T (p.Tyr327Phe)
11g.47346299T>CCA380331502MYBPC3c.998A>G (p.Tyr333Cys)
c.980A>G (p.Tyr327Cys)
11g.47346299T>GCA380331500MYBPC3c.998A>C (p.Tyr333Ser)
c.980A>C (p.Tyr327Ser)
11g.47346300A>CCA380331504MYBPC3c.997T>G (p.Tyr333Asp)
c.979T>G (p.Tyr327Asp)
11g.47346300A>GCA380331508MYBPC3c.997T>C (p.Tyr333His)
c.979T>C (p.Tyr327His)
11g.47346300A>TCA380331506MYBPC3c.997T>A (p.Tyr333Asn)
c.979T>A (p.Tyr327Asn)
11g.47346301C>ACA380331511MYBPC3c.996G>T (p.Glu332Asp)
c.978G>T (p.Glu326Asp)
11g.47346301C>GCA380331513MYBPC3c.996G>C (p.Glu332Asp)
c.978G>C (p.Glu326Asp)
11g.47346301C>TCA474220921MYBPC3c.996G>A (p.Glu332=)
c.978G>A (p.Glu326=)
11g.47346302T>ACA380331515MYBPC3c.995A>T (p.Glu332Val)
c.977A>T (p.Glu326Val)
11g.47346302T>CCA380331517MYBPC3c.995A>G (p.Glu332Gly)
c.977A>G (p.Glu326Gly)
11g.47346302T>GCA380331519MYBPC3c.995A>C (p.Glu332Ala)
c.977A>C (p.Glu326Ala)
11g.47346303C>ACA16616724MYBPC3c.994G>T (p.Glu332Ter)
c.976G>T (p.Glu326Ter)
11g.47346303C=CA1969339637MYBPC3c.994G= (p.Glu332=)
c.976G= (p.Glu326=)
11g.47346303C>GCA380331523MYBPC3c.994G>C (p.Glu332Gln)
c.976G>C (p.Glu326Gln)
11g.47346303C>TCA016247MYBPC3c.994G>A (p.Glu332Lys)
c.976G>A (p.Glu326Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47346304A>CCA474220927MYBPC3c.993T>G (p.Ser331=)
c.975T>G (p.Ser325=)
11g.47346304A>GCA474220928MYBPC3c.993T>C (p.Ser331=)
c.975T>C (p.Ser325=)
11g.47346304A>TCA474220929MYBPC3c.993T>A (p.Ser331=)
c.975T>A (p.Ser325=)
11g.47346304dupCA016238MYBPC3c.993dup (p.Glu332Ter)
c.975dup (p.Glu326Ter)
ClinVar dbSNP
11g.47346305G>ACA380331530MYBPC3c.992C>T (p.Ser331Phe)
c.974C>T (p.Ser325Phe)
11g.47346305G>CCA380331533MYBPC3c.992C>G (p.Ser331Cys)
c.974C>G (p.Ser325Cys)

Number of alleles fetched