Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47341257_47344691delCA913203384MYBPC3c.1091-1066_1791-12del
c.1073-1066_1773-12del
11g.47342513_47342744delCA2580084236MYBPC3c.1460_1624+67del
c.1442_1606+67del
ClinVar
11g.47342650T>ACA380325119MYBPC3c.1552A>T (p.Met518Leu)
c.1534A>T (p.Met512Leu)
11g.47342650T>CCA380325120MYBPC3c.1552A>G (p.Met518Val)
c.1534A>G (p.Met512Val)
dbSNP gnomAD v3 gnomAD v4
11g.47342650T>GCA380325121MYBPC3c.1552A>C (p.Met518Leu)
c.1534A>C (p.Met512Leu)
11g.47342650T=CA1969335891MYBPC3c.1552A= (p.Met518=)
c.1534A= (p.Met512=)
11g.47342651G>ACA474219780MYBPC3c.1551C>T (p.Ala517=)
c.1533C>T (p.Ala511=)
11g.47342651G>CCA474219781MYBPC3c.1551C>G (p.Ala517=)
c.1533C>G (p.Ala511=)
dbSNP
11g.47342651G=CA1969335892MYBPC3c.1551C= (p.Ala517=)
c.1533C= (p.Ala511=)
11g.47342651G>TCA474219782MYBPC3c.1551C>A (p.Ala517=)
c.1533C>A (p.Ala511=)
11g.47342651_47342652insTCCA2548150362MYBPC3c.1550_1551insGA (p.Met518ThrfsTer?)
c.1532_1533insGA (p.Met512ThrfsTer?)
11g.47342652G>ACA380325124MYBPC3c.1550C>T (p.Ala517Val)
c.1532C>T (p.Ala511Val)
11g.47342652G>CCA380325123MYBPC3c.1550C>G (p.Ala517Gly)
c.1532C>G (p.Ala511Gly)
11g.47342652G>TCA380325122MYBPC3c.1550C>A (p.Ala517Asp)
c.1532C>A (p.Ala511Asp)
11g.47342652_47342655delinsGCCTCA1969335894MYBPC3c.1547_1550delinsAGGC (p.Glu516=)
c.1529_1532delinsAGGC (p.Glu510=)
11g.47342653C>ACA380325125MYBPC3c.1549G>T (p.Ala517Ser)
c.1531G>T (p.Ala511Ser)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47342653C=CA1969335896MYBPC3c.1549G= (p.Ala517=)
c.1531G= (p.Ala511=)
11g.47342653C>GCA380325126MYBPC3c.1549G>C (p.Ala517Pro)
c.1531G>C (p.Ala511Pro)
dbSNP gnomAD v4
11g.47342653C>TCA380325127MYBPC3c.1549G>A (p.Ala517Thr)
c.1531G>A (p.Ala511Thr)
gnomAD v4
11g.47342654_47342656delCA010626MYBPC3c.1547_1549del (p.Glu516del)
c.1529_1531del (p.Glu510del)
dbSNP
11g.47342654C>ACA380325128MYBPC3c.1548G>T (p.Glu516Asp)
c.1530G>T (p.Glu510Asp)
11g.47342654C=CA1969335898MYBPC3c.1548G= (p.Glu516=)
c.1530G= (p.Glu510=)
11g.47342654C>GCA380325129MYBPC3c.1548G>C (p.Glu516Asp)
c.1530G>C (p.Glu510Asp)
ClinVar dbSNP
11g.47342654C>TCA474219792MYBPC3c.1548G>A (p.Glu516=)
c.1530G>A (p.Glu510=)
ClinVar dbSNP
11g.47342655T>ACA380325130MYBPC3c.1547A>T (p.Glu516Val)
c.1529A>T (p.Glu510Val)
11g.47342655T>CCA380325131MYBPC3c.1547A>G (p.Glu516Gly)
c.1529A>G (p.Glu510Gly)
11g.47342655T>GCA380325132MYBPC3c.1547A>C (p.Glu516Ala)
c.1529A>C (p.Glu510Ala)
11g.47342656_47342659delCA078158MYBPC3c.1544_1547del (p.Asn515ArgfsTer?)
c.1526_1529del (p.Asn509ArgfsTer?)
11g.47342656C>ACA380325133MYBPC3c.1546G>T (p.Glu516Ter)
c.1528G>T (p.Glu510Ter)
ClinVar dbSNP gnomAD v4
11g.47342656C=CA1969335900MYBPC3c.1546G= (p.Glu516=)
c.1528G= (p.Glu510=)
11g.47342656C>GCA380325134MYBPC3c.1546G>C (p.Glu516Gln)
c.1528G>C (p.Glu510Gln)
11g.47342656C>TCA010618MYBPC3c.1546G>A (p.Glu516Lys)
c.1528G>A (p.Glu510Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47342656_47342659delinsCGTTCA1969335902MYBPC3c.1543_1546delinsAACG (p.Asn515=)
c.1525_1528delinsAACG (p.Asn509=)
11g.47342657G>ACA078163MYBPC3c.1545C>T (p.Asn515=)
c.1527C>T (p.Asn509=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11g.47342657G>CCA380325136MYBPC3c.1545C>G (p.Asn515Lys)
c.1527C>G (p.Asn509Lys)
11g.47342657G=CA1969335904MYBPC3c.1545C= (p.Asn515=)
c.1527C= (p.Asn509=)
11g.47342657G>TCA380325135MYBPC3c.1545C>A (p.Asn515Lys)
c.1527C>A (p.Asn509Lys)
11g.47342658_47342660delCA010600MYBPC3c.1543_1545del (p.Asn515del)
c.1525_1527del (p.Asn509del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47342658T>ACA380325137MYBPC3c.1544A>T (p.Asn515Ile)
c.1526A>T (p.Asn509Ile)
11g.47342658T>CCA010609MYBPC3c.1544A>G (p.Asn515Ser)
c.1526A>G (p.Asn509Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47342658T>GCA380325138MYBPC3c.1544A>C (p.Asn515Thr)
c.1526A>C (p.Asn509Thr)
11g.47342658T=CA1969335905MYBPC3c.1544A= (p.Asn515=)
c.1526A= (p.Asn509=)
11g.47342659_47342662delCA045666MYBPC3c.1541_1544del (p.Ile514ThrfsTer?)
c.1523_1526del (p.Ile508ThrfsTer?)
11g.47342659T>ACA380325139MYBPC3c.1543A>T (p.Asn515Tyr)
c.1525A>T (p.Asn509Tyr)
11g.47342659T>CCA380325140MYBPC3c.1543A>G (p.Asn515Asp)
c.1525A>G (p.Asn509Asp)
11g.47342659T>GCA380325141MYBPC3c.1543A>C (p.Asn515His)
c.1525A>C (p.Asn509His)
gnomAD v4
11g.47342663_47342665delCA2580615690MYBPC3c.1541_1543del (p.Ile514del)
c.1523_1525del (p.Ile508del)
ClinVar dbSNP
11g.47342660G>ACA045711MYBPC3c.1542C>T (p.Ile514=)
c.1524C>T (p.Ile508=)
11g.47342660G>CCA380325142MYBPC3c.1542C>G (p.Ile514Met)
c.1524C>G (p.Ile508Met)
11g.47342660G>TCA474219825MYBPC3c.1542C>A (p.Ile514=)
c.1524C>A (p.Ile508=)

Number of alleles fetched