Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23416250C>ACA015240MHRT,MYH7c.4707G>T (p.Lys1569Asn)
n.511C>A
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23416250C=CA2123465907MHRT,MYH7c.4707G= (p.Lys1569=)
n.511C=
14g.23416250C>GCA043659MHRT,MYH7c.4707G>C (p.Lys1569Asn)
n.511C>G
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23416250C>TCA485766417MHRT,MYH7c.4707G>A (p.Lys1569=)
n.511C>T
14g.23416251T>ACA389037811MHRT,MYH7c.4706A>T (p.Lys1569Met)
n.512T>A
14g.23416251T>CCA389037812MHRT,MYH7c.4706A>G (p.Lys1569Arg)
n.512T>C
14g.23416251T>GCA389037813MHRT,MYH7c.4706A>C (p.Lys1569Thr)
n.512T>G
14g.23416252T>ACA389037814MHRT,MYH7c.4705A>T (p.Lys1569Ter)
n.513T>A
14g.23416252T>CCA389037815MHRT,MYH7c.4705A>G (p.Lys1569Glu)
n.513T>C
14g.23416252T>GCA389037816MHRT,MYH7c.4705A>C (p.Lys1569Gln)
n.513T>G
14g.23416253G>ACA485766419MHRT,MYH7c.4704C>T (p.Ile1568=)
n.514G>A
14g.23416253G>CCA389037817MHRT,MYH7c.4704C>G (p.Ile1568Met)
n.514G>C
14g.23416253G>TCA485766420MHRT,MYH7c.4704C>A (p.Ile1568=)
n.514G>T
ClinVar
14g.23416254A>CCA389037818MHRT,MYH7c.4703T>G (p.Ile1568Ser)
n.515A>C
14g.23416254A>GCA389037819MHRT,MYH7c.4703T>C (p.Ile1568Thr)
n.515A>G
14g.23416254A>TCA389037820MHRT,MYH7c.4703T>A (p.Ile1568Asn)
n.515A>T
14g.23416255T>ACA389037821MHRT,MYH7c.4702A>T (p.Ile1568Phe)
n.516T>A
14g.23416255T>CCA389037823MHRT,MYH7c.4702A>G (p.Ile1568Val)
n.516T>C
ClinVar dbSNP
14g.23416255T>GCA389037822MHRT,MYH7c.4702A>C (p.Ile1568Leu)
n.516T>G
14g.23416255T=CA2123465914MHRT,MYH7c.4702A= (p.Ile1568=)
n.516T=
14g.23416256C>ACA389037824MHRT,MYH7c.4701G>T (p.Gln1567His)
n.517C>A
14g.23416256C=CA2123465918MHRT,MYH7c.4701G= (p.Gln1567=)
n.517C=
14g.23416256C>GCA389037825MHRT,MYH7c.4701G>C (p.Gln1567His)
n.517C>G
ClinVar dbSNP
14g.23416256C>TCA485766422MHRT,MYH7c.4701G>A (p.Gln1567=)
n.517C>T
14g.23416257T>ACA389037826MHRT,MYH7c.4700A>T (p.Gln1567Leu)
n.518T>A
14g.23416257T>CCA389037827MHRT,MYH7c.4700A>G (p.Gln1567Arg)
n.518T>C
14g.23416257T>GCA389037828MHRT,MYH7c.4700A>C (p.Gln1567Pro)
n.518T>G
ClinVar COSMIC
14g.23416258G>ACA389037829MHRT,MYH7c.4699C>T (p.Gln1567Ter)
n.519G>A
ClinVar dbSNP gnomAD v4
14g.23416258G>CCA389037830MHRT,MYH7c.4699C>G (p.Gln1567Glu)
n.519G>C
14g.23416258G=CA2123465922MHRT,MYH7c.4699C= (p.Gln1567=)
n.519G=
14g.23416258G>TCA389037831MHRT,MYH7c.4699C>A (p.Gln1567Lys)
n.519G>T
14g.23416259G>ACA485766423MHRT,MYH7c.4698C>T (p.Asn1566=)
n.520G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23416259G>CCA389037832MHRT,MYH7c.4698C>G (p.Asn1566Lys)
n.520G>C
14g.23416259G=CA2123465931MHRT,MYH7c.4698C= (p.Asn1566=)
n.520G=
14g.23416259G>TCA389037833MHRT,MYH7c.4698C>A (p.Asn1566Lys)
n.520G>T
14g.23416260T>ACA389037834MHRT,MYH7c.4697A>T (p.Asn1566Ile)
n.521T>A
14g.23416260T>CCA257810700MHRT,MYH7c.4697A>G (p.Asn1566Ser)
n.521T>C
ClinVar dbSNP gnomAD v4
14g.23416260T>GCA389037835MHRT,MYH7c.4697A>C (p.Asn1566Thr)
n.521T>G
14g.23416260T=CA2123465941MHRT,MYH7c.4697A= (p.Asn1566=)
n.521T=
14g.23416261T>ACA389037836MHRT,MYH7c.4696A>T (p.Asn1566Tyr)
n.522T>A
14g.23416261T>CCA389037838MHRT,MYH7c.4696A>G (p.Asn1566Asp)
n.522T>C
14g.23416261T>GCA389037837MHRT,MYH7c.4696A>C (p.Asn1566His)
n.522T>G
14g.23416262G>ACA485766428MHRT,MYH7c.4695C>T (p.Phe1565=)
n.523G>A
14g.23416262G>CCA389037839MHRT,MYH7c.4695C>G (p.Phe1565Leu)
n.523G>C
14g.23416262G>TCA389037840MHRT,MYH7c.4695C>A (p.Phe1565Leu)
n.523G>T
14g.23416263A>CCA389037841MHRT,MYH7c.4694T>G (p.Phe1565Cys)
n.524A>C
14g.23416263A>GCA389037842MHRT,MYH7c.4694T>C (p.Phe1565Ser)
n.524A>G
14g.23416263A>TCA389037843MHRT,MYH7c.4694T>A (p.Phe1565Tyr)
n.524A>T
14g.23416264A>CCA389037844MHRT,MYH7c.4693T>G (p.Phe1565Val)
n.525A>C
gnomAD v3 gnomAD v4
14g.23416264A>GCA389037845MHRT,MYH7c.4693T>C (p.Phe1565Leu)
n.525A>G
gnomAD v4
14g.23416264A>TCA389037846MHRT,MYH7c.4693T>A (p.Phe1565Ile)
n.525A>T
14g.23416265C>ACA389037847MHRT,MYH7c.4692G>T (p.Glu1564Asp)
n.526C>A
14g.23416265C>GCA389037848MHRT,MYH7c.4692G>C (p.Glu1564Asp)
n.526C>G
14g.23416265C>TCA485766434MHRT,MYH7c.4692G>A (p.Glu1564=)
n.526C>T
14g.23416266T>ACA389037851MHRT,MYH7c.4691A>T (p.Glu1564Val)
n.527T>A
14g.23416266T>CCA389037850MHRT,MYH7c.4691A>G (p.Glu1564Gly)
n.527T>C
14g.23416266T>GCA389037849MHRT,MYH7c.4691A>C (p.Glu1564Ala)
n.527T>G
ClinVar
14g.23416267C>ACA389037852MHRT,MYH7c.4690G>T (p.Glu1564Ter)
n.528C>A
14g.23416267C>GCA389037854MHRT,MYH7c.4690G>C (p.Glu1564Gln)
n.528C>G
gnomAD v4
14g.23416267C>TCA389037853MHRT,MYH7c.4690G>A (p.Glu1564Lys)
n.528C>T
14g.23416268C>ACA485766436MHRT,MYH7c.4689G>T (p.Leu1563=)
n.529C>A
14g.23416268C=CA2123465965MHRT,MYH7c.4689G= (p.Leu1563=)
n.529C=
14g.23416268C>GCA485766435MHRT,MYH7c.4689G>C (p.Leu1563=)
n.529C>G
ClinVar dbSNP
14g.23416268C>TCA043646MHRT,MYH7c.4689G>A (p.Leu1563=)
n.529C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23416269A>CCA389037857MHRT,MYH7c.4688T>G (p.Leu1563Arg)
n.530A>C
14g.23416269A>GCA389037855MHRT,MYH7c.4688T>C (p.Leu1563Pro)
n.530A>G
14g.23416269A>TCA389037856MHRT,MYH7c.4688T>A (p.Leu1563Gln)
n.530A>T
14g.23416270G>ACA485766439MHRT,MYH7c.4687C>T (p.Leu1563=)
n.531G>A
14g.23416270G>CCA015233MHRT,MYH7c.4687C>G (p.Leu1563Val)
n.531G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23416270G=CA2123465976MHRT,MYH7c.4687C= (p.Leu1563=)
n.531G=
14g.23416270G>TCA389037858MHRT,MYH7c.4687C>A (p.Leu1563Met)
n.531G>T
14g.23416271C>ACA389037859MHRT,MYH7c.4686G>T (p.Gln1562His)
n.532C>A
14g.23416271C>GCA389037860MHRT,MYH7c.4686G>C (p.Gln1562His)
n.532C>G
14g.23416271C>TCA485766444MHRT,MYH7c.4686G>A (p.Gln1562=)
n.532C>T
ClinVar dbSNP
14g.23416271_23416287delinsCTGGGCCCGGAGGATCTCA2123465986MHRT,MYH7c.4670_4686delinsAGATCCTCCGGGCCCAG (p.Lys1557=)
n.532_548delinsCTGGGCCCGGAGGATCT
14g.23416272T>ACA389037861MHRT,MYH7c.4685A>T (p.Gln1562Leu)
n.533T>A
14g.23416272T>CCA389037862MHRT,MYH7c.4685A>G (p.Gln1562Arg)
n.533T>C
14g.23416272T>GCA389037863MHRT,MYH7c.4685A>C (p.Gln1562Pro)
n.533T>G
14g.23416274_23416289delCA043479MHRT,MYH7c.4670_4685del (p.Lys1557SerfsTer?)
n.535_550del
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23416273G>ACA389037866MHRT,MYH7c.4684C>T (p.Gln1562Ter)
n.534G>A
dbSNP gnomAD v2 gnomAD v4
14g.23416273G>CCA389037865MHRT,MYH7c.4684C>G (p.Gln1562Glu)
n.534G>C
dbSNP gnomAD v2 gnomAD v4
14g.23416273G=CA2123465994MHRT,MYH7c.4684C= (p.Gln1562=)
n.534G=
14g.23416273G>TCA389037864MHRT,MYH7c.4684C>A (p.Gln1562Lys)
n.534G>T
gnomAD v4
14g.23416274G>ACA485766450MHRT,MYH7c.4683C>T (p.Ala1561=)
n.535G>A
gnomAD v4
14g.23416274G>CCA485766451MHRT,MYH7c.4683C>G (p.Ala1561=)
n.535G>C
14g.23416274G=CA2123465998MHRT,MYH7c.4683C= (p.Ala1561=)
n.535G=
14g.23416274G>TCA043625MHRT,MYH7c.4683C>A (p.Ala1561=)
n.535G>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23416275G>ACA389037867MHRT,MYH7c.4682C>T (p.Ala1561Val)
n.536G>A
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23416275G>CCA389037868MHRT,MYH7c.4682C>G (p.Ala1561Gly)
n.536G>C
14g.23416275G=CA2123466004MHRT,MYH7c.4682C= (p.Ala1561=)
n.536G=
14g.23416275G>TCA389037869MHRT,MYH7c.4682C>A (p.Ala1561Asp)
n.536G>T
gnomAD v4
14g.23416275_23416276delinsGCCA2123466007MHRT,MYH7c.4681_4682delinsGC (p.Ala1561=)
n.536_537delinsGC
14g.23416276C>ACA389037870MHRT,MYH7c.4681G>T (p.Ala1561Ser)
n.537C>A
ClinVar gnomAD v4
14g.23416276C=CA2123466015MHRT,MYH7c.4681G= (p.Ala1561=)
n.537C=
14g.23416276C>GCA16619846MHRT,MYH7c.4681G>C (p.Ala1561Pro)
n.537C>G
ClinVar dbSNP
14g.23416276C>TCA389037871MHRT,MYH7c.4681G>A (p.Ala1561Thr)
n.537C>T
14g.23416278delCA613317654MHRT,MYH7c.4681del (p.Ala1561ProfsTer?)
n.539del
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23416277C>ACA485766457MHRT,MYH7c.4680G>T (p.Arg1560=)
n.538C>A
14g.23416277C=CA2123466023MHRT,MYH7c.4680G= (p.Arg1560=)
n.538C=
14g.23416277C>GCA485766458MHRT,MYH7c.4680G>C (p.Arg1560=)
n.538C>G
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
14g.23416277C>TCA043587MHRT,MYH7c.4680G>A (p.Arg1560=)
n.538C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23416278C>ACA389037872MHRT,MYH7c.4679G>T (p.Arg1560Leu)
n.539C>A
14g.23416278C=CA2123466037MHRT,MYH7c.4679G= (p.Arg1560=)
n.539C=
14g.23416278C>GCA389037873MHRT,MYH7c.4679G>C (p.Arg1560Pro)
n.539C>G
ClinVar dbSNP
14g.23416278C>TCA015224MHRT,MYH7c.4679G>A (p.Arg1560Gln)
n.539C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23416279G>ACA043564MHRT,MYH7c.4678C>T (p.Arg1560Trp)
n.540G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
14g.23416279G>CCA389037874MHRT,MYH7c.4678C>G (p.Arg1560Gly)
n.540G>C
14g.23416279G=CA2123466049MHRT,MYH7c.4678C= (p.Arg1560=)
n.540G=
14g.23416279G>TCA043550MHRT,MYH7c.4678C>A (p.Arg1560=)
n.540G>T
dbSNP ExAC gnomAD v2
14g.23416280G>ACA043534MHRT,MYH7c.4677C>T (p.Leu1559=)
n.541G>A
dbSNP ExAC gnomAD v2
14g.23416280G>CCA485766462MHRT,MYH7c.4677C>G (p.Leu1559=)
n.541G>C
gnomAD v4
14g.23416280G=CA2123466057MHRT,MYH7c.4677C= (p.Leu1559=)
n.541G=
14g.23416280G>TCA043517MHRT,MYH7c.4677C>A (p.Leu1559=)
n.541G>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23416281A>CCA389037875MHRT,MYH7c.4676T>G (p.Leu1559Arg)
n.542A>C
14g.23416281A>GCA389037876MHRT,MYH7c.4676T>C (p.Leu1559Pro)
n.542A>G
14g.23416281A>TCA389037877MHRT,MYH7c.4676T>A (p.Leu1559His)
n.542A>T
14g.23416282G>ACA389037878MHRT,MYH7c.4675C>T (p.Leu1559Phe)
n.543G>A
14g.23416282G>CCA389037879MHRT,MYH7c.4675C>G (p.Leu1559Val)
n.543G>C
14g.23416282G>TCA389037880MHRT,MYH7c.4675C>A (p.Leu1559Ile)
n.543G>T
14g.23416283G>ACA485766464MHRT,MYH7c.4674C>T (p.Ile1558=)
n.544G>A
ClinVar dbSNP COSMIC
14g.23416283G>CCA389037881MHRT,MYH7c.4674C>G (p.Ile1558Met)
n.544G>C
gnomAD v4
14g.23416283G>TCA485766465MHRT,MYH7c.4674C>A (p.Ile1558=)
n.544G>T
14g.23416284A=CA2123466069MHRT,MYH7c.4673T= (p.Ile1558=)
n.545A=
14g.23416284A>CCA257810745MHRT,MYH7c.4673T>G (p.Ile1558Ser)
n.545A>C
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23416284A>GCA389037882MHRT,MYH7c.4673T>C (p.Ile1558Thr)
n.545A>G
14g.23416284A>TCA389037883MHRT,MYH7c.4673T>A (p.Ile1558Asn)
n.545A>T
14g.23416285T>ACA043503MHRT,MYH7c.4672A>T (p.Ile1558Phe)
n.546T>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23416285T>CCA389037884MHRT,MYH7c.4672A>G (p.Ile1558Val)
n.546T>C
14g.23416285T>GCA389037885MHRT,MYH7c.4672A>C (p.Ile1558Leu)
n.546T>G
14g.23416285T=CA2123466077MHRT,MYH7c.4672A= (p.Ile1558=)
n.546T=
14g.23416286C>ACA389037886MHRT,MYH7c.4671G>T (p.Lys1557Asn)
n.547C>A
ClinVar COSMIC
14g.23416286C=CA2123466087MHRT,MYH7c.4671G= (p.Lys1557=)
n.547C=
14g.23416286C>GCA389037887MHRT,MYH7c.4671G>C (p.Lys1557Asn)
n.547C>G
14g.23416286C>TCA015216MHRT,MYH7c.4671G>A (p.Lys1557=)
n.547C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23416287T>ACA389037888MHRT,MYH7c.4670A>T (p.Lys1557Met)
n.548T>A
14g.23416287T>CCA389037889MHRT,MYH7c.4670A>G (p.Lys1557Arg)
n.548T>C
ClinVar dbSNP
14g.23416287T>GCA389037890MHRT,MYH7c.4670A>C (p.Lys1557Thr)
n.548T>G
14g.23416287T=CA2123466096MHRT,MYH7c.4670A= (p.Lys1557=)
n.548T=
14g.23416288T>ACA389037891MHRT,MYH7c.4669A>T (p.Lys1557Ter)
n.549T>A
14g.23416288T>CCA389037892MHRT,MYH7c.4669A>G (p.Lys1557Glu)
n.549T>C
14g.23416288T>GCA389037893MHRT,MYH7c.4669A>C (p.Lys1557Gln)
n.549T>G
14g.23416289G>ACA485766468MHRT,MYH7c.4668C>T (p.Gly1556=)
n.550G>A
14g.23416289G>CCA485766471MHRT,MYH7c.4668C>G (p.Gly1556=)
n.550G>C
14g.23416289G=CA2123466101MHRT,MYH7c.4668C= (p.Gly1556=)
n.550G=
14g.23416289G>TCA043470MHRT,MYH7c.4668C>A (p.Gly1556=)
n.550G>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23416290C>ACA389037894MHRT,MYH7c.4667G>T (p.Gly1556Val)
n.551C>A
14g.23416290C=CA2123466109MHRT,MYH7c.4667G= (p.Gly1556=)
n.551C=
14g.23416290C>GCA389037895MHRT,MYH7c.4667G>C (p.Gly1556Ala)
n.551C>G
14g.23416290C>TCA389037896MHRT,MYH7c.4667G>A (p.Gly1556Asp)
n.551C>T
ClinVar dbSNP
14g.23416291C>ACA389037898MHRT,MYH7c.4666G>T (p.Gly1556Cys)
n.552C>A
dbSNP
14g.23416291C=CA2123466118MHRT,MYH7c.4666G= (p.Gly1556=)
n.552C=
14g.23416291C>GCA389037899MHRT,MYH7c.4666G>C (p.Gly1556Arg)
n.552C>G
14g.23416291C>TCA389037897MHRT,MYH7c.4666G>A (p.Gly1556Ser)
n.552C>T
14g.23416292C>ACA389037901MHRT,MYH7c.4665G>T (p.Glu1555Asp)
n.553C>A
14g.23416292C=CA2123466125MHRT,MYH7c.4665G= (p.Glu1555=)
n.553C=
14g.23416292C>GCA389037900MHRT,MYH7c.4665G>C (p.Glu1555Asp)
n.553C>G
14g.23416292C>TCA485766473MHRT,MYH7c.4665G>A (p.Glu1555=)
n.553C>T
ClinVar dbSNP
14g.23416293T>ACA389037902MHRT,MYH7c.4664A>T (p.Glu1555Val)
n.554T>A
14g.23416293T>CCA015211MHRT,MYH7c.4664A>G (p.Glu1555Gly)
n.554T>C
ClinVar dbSNP gnomAD v4
14g.23416293T>GCA389037903MHRT,MYH7c.4664A>C (p.Glu1555Ala)
n.554T>G
14g.23416293T=CA2123466131MHRT,MYH7c.4664A= (p.Glu1555=)
n.554T=
14g.23416294C>ACA389037904MHRT,MYH7c.4663G>T (p.Glu1555Ter)
n.555C>A
14g.23416294C=CA2123466138MHRT,MYH7c.4663G= (p.Glu1555=)
n.555C=
14g.23416294C>GCA015206MHRT,MYH7c.4663G>C (p.Glu1555Gln)
n.555C>G
ClinVar dbSNP
14g.23416294C>TCA389037905MHRT,MYH7c.4663G>A (p.Glu1555Lys)
n.555C>T
ClinVar dbSNP COSMIC
14g.23416295C>ACA389037906MHRT,MYH7c.4662G>T (p.Glu1554Asp)
n.556C>A
14g.23416295C=CA2123466147MHRT,MYH7c.4662G= (p.Glu1554=)
n.556C=
14g.23416295C>GCA389037907MHRT,MYH7c.4662G>C (p.Glu1554Asp)
n.556C>G
14g.23416295C>TCA043454MHRT,MYH7c.4662G>A (p.Glu1554=)
n.556C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23416296T>ACA389037908MHRT,MYH7c.4661A>T (p.Glu1554Val)
n.557T>A
14g.23416296T>CCA389037909MHRT,MYH7c.4661A>G (p.Glu1554Gly)
n.557T>C
14g.23416296T>GCA389037910MHRT,MYH7c.4661A>C (p.Glu1554Ala)
n.557T>G
14g.23416297C>ACA389037911MHRT,MYH7c.4660G>T (p.Glu1554Ter)
n.558C>A
14g.23416297C=CA2123466153MHRT,MYH7c.4660G= (p.Glu1554=)
n.558C=
14g.23416297C>GCA043434MHRT,MYH7c.4660G>C (p.Glu1554Gln)
n.558C>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23416297C>TCA389037912MHRT,MYH7c.4660G>A (p.Glu1554Lys)
n.558C>T
ClinVar dbSNP gnomAD v4
14g.23416298G>ACA043411MHRT,MYH7c.4659C>T (p.His1553=)
n.558+1G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23416298G>CCA389037913MHRT,MYH7c.4659C>G (p.His1553Gln)
n.558+1G>C
ClinVar
14g.23416298G=CA2123466161MHRT,MYH7c.4659C= (p.His1553=)
n.558+1G=
14g.23416298G>TCA389037914MHRT,MYH7c.4659C>A (p.His1553Gln)
n.558+1G>T
14g.23416299T>ACA389037915MHRT,MYH7c.4658A>T (p.His1553Leu)
n.558+2T>A
14g.23416299T>CCA389037916MHRT,MYH7c.4658A>G (p.His1553Arg)
n.558+2T>C
14g.23416299T>GCA389037917MHRT,MYH7c.4658A>C (p.His1553Pro)
n.558+2T>G
14g.23416300G>ACA389037918MHRT,MYH7c.4657C>T (p.His1553Tyr)
n.558+3G>A
14g.23416300G>CCA389037919MHRT,MYH7c.4657C>G (p.His1553Asp)
n.558+3G>C
14g.23416300G>TCA389037920MHRT,MYH7c.4657C>A (p.His1553Asn)
n.558+3G>T
14g.23416301C>ACA043403MHRT,MYH7c.4656G>T (p.Glu1552Asp)
n.558+4C>A
ClinVar dbSNP ExAC gnomAD v2
14g.23416301C=CA2123466175MHRT,MYH7c.4656G= (p.Glu1552=)
n.558+4C=
14g.23416301C>GCA389037921MHRT,MYH7c.4656G>C (p.Glu1552Asp)
n.558+4C>G
14g.23416301C>TCA485766478MHRT,MYH7c.4656G>A (p.Glu1552=)
n.558+4C>T
dbSNP
14g.23416302T>ACA389037923MHRT,MYH7c.4655A>T (p.Glu1552Val)
n.558+5T>A
14g.23416302T>CCA389037924MHRT,MYH7c.4655A>G (p.Glu1552Gly)
n.558+5T>C
14g.23416302T>GCA389037922MHRT,MYH7c.4655A>C (p.Glu1552Ala)
n.558+5T>G
14g.23416302_23416304delinsAGGAGGCA2580087886MHRT,MYH7c.4653_4655delinsCCTCCT (p.Glu1552delinsLeuLeu)
n.558+5_558+7delinsAGGAGG
ClinVar
14g.23416303C>ACA389037925MHRT,MYH7c.4654G>T (p.Glu1552Ter)
n.558+6C>A
14g.23416303C>GCA389037926MHRT,MYH7c.4654G>C (p.Glu1552Gln)
n.558+6C>G
14g.23416303C>TCA389037927MHRT,MYH7c.4654G>A (p.Glu1552Lys)
n.558+6C>T
14g.23416304C>ACA485766479MHRT,MYH7c.4653G>T (p.Leu1551=)
n.558+7C>A
14g.23416304C>GCA485766480MHRT,MYH7c.4653G>C (p.Leu1551=)
n.558+7C>G
ClinVar
14g.23416304C>TCA485766481MHRT,MYH7c.4653G>A (p.Leu1551=)
n.558+7C>T
14g.23416305A>CCA389037928MHRT,MYH7c.4652T>G (p.Leu1551Arg)
n.558+8A>C
14g.23416305A>GCA389037929MHRT,MYH7c.4652T>C (p.Leu1551Pro)
n.558+8A>G
ClinVar
14g.23416305A>TCA389037930MHRT,MYH7c.4652T>A (p.Leu1551Gln)
n.558+8A>T
14g.23416306G>ACA485766482MHRT,MYH7c.4651C>T (p.Leu1551=)
n.558+9G>A
ClinVar dbSNP
14g.23416306G>CCA389037932MHRT,MYH7c.4651C>G (p.Leu1551Val)
n.558+9G>C
14g.23416306G>TCA389037931MHRT,MYH7c.4651C>A (p.Leu1551Met)
n.558+9G>T
14g.23416307G>ACA257810773MHRT,MYH7c.4650C>T (p.Ser1550=)
n.558+10G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23416307G>CCA485766483MHRT,MYH7c.4650C>G (p.Ser1550=)
n.558+10G>C
14g.23416307G=CA2123466183MHRT,MYH7c.4650C= (p.Ser1550=)
n.558+10G=
14g.23416307G>TCA485766484MHRT,MYH7c.4650C>A (p.Ser1550=)
n.558+10G>T
14g.23416308G>ACA015196MHRT,MYH7c.4649C>T (p.Ser1550Phe)
n.558+11G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23416308G>CCA389037933MHRT,MYH7c.4649C>G (p.Ser1550Cys)
n.558+11G>C
14g.23416308G=CA2123466193MHRT,MYH7c.4649C= (p.Ser1550=)
n.558+11G=
14g.23416308G>TCA389037934MHRT,MYH7c.4649C>A (p.Ser1550Tyr)
n.558+11G>T
14g.23416309A=CA2123466204MHRT,MYH7c.4648T= (p.Ser1550=)
n.558+12A=
14g.23416309A>CCA389037935MHRT,MYH7c.4648T>G (p.Ser1550Ala)
n.558+12A>C
14g.23416309A>GCA389037936MHRT,MYH7c.4648T>C (p.Ser1550Pro)
n.558+12A>G
ClinVar dbSNP
14g.23416309A>TCA389037937MHRT,MYH7c.4648T>A (p.Ser1550Thr)
n.558+12A>T
14g.23416310G>ACA043394MHRT,MYH7c.4647C>T (p.Ala1549=)
n.558+13G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23416310G>CCA485766489MHRT,MYH7c.4647C>G (p.Ala1549=)
n.558+13G>C
14g.23416310G=CA2123466214MHRT,MYH7c.4647C= (p.Ala1549=)
n.558+13G=
14g.23416310G>TCA485766488MHRT,MYH7c.4647C>A (p.Ala1549=)
n.558+13G>T
14g.23416311G>ACA389037938MHRT,MYH7c.4646C>T (p.Ala1549Val)
n.558+14G>A
14g.23416311G>CCA389037940MHRT,MYH7c.4646C>G (p.Ala1549Gly)
n.558+14G>C
ClinVar dbSNP
14g.23416311G=CA2123466222MHRT,MYH7c.4646C= (p.Ala1549=)
n.558+14G=
14g.23416311G>TCA389037939MHRT,MYH7c.4646C>A (p.Ala1549Asp)
n.558+14G>T
ClinVar gnomAD v4
14g.23416312C>ACA389037941MHRT,MYH7c.4645G>T (p.Ala1549Ser)
n.558+15C>A
14g.23416312C>GCA389037942MHRT,MYH7c.4645G>C (p.Ala1549Pro)
n.558+15C>G
14g.23416312C>TCA389037943MHRT,MYH7c.4645G>A (p.Ala1549Thr)
n.558+15C>T
14g.23416313C>ACA389037944MHRT,MYH7c.4645-1G>T (n.4645-1G>T)
n.558+16C>A
14g.23416313C>GCA389037945MHRT,MYH7c.4645-1G>C (n.4645-1G>C)
n.558+16C>G
ClinVar
14g.23416313C>TCA389037946MHRT,MYH7c.4645-1G>A (n.4645-1G>A)
n.558+16C>T
ClinVar
14g.23416314T>ACA389037947MHRT,MYH7c.4645-2A>T (n.4645-2A>T)
n.558+17T>A
ClinVar dbSNP
14g.23416314T>CCA389037948MHRT,MYH7c.4645-2A>G (n.4645-2A>G)
n.558+17T>C
gnomAD v4
14g.23416314T>GCA389037949MHRT,MYH7c.4645-2A>C (n.4645-2A>C)
n.558+17T>G
14g.23416314T=CA2123466234MHRT,MYH7c.4645-2A= (n.4645-2A=)
n.558+17T=
14g.23416314_23416315insCCA2624234785MHRT,MYH7c.4645-3_4645-2insG (n.4645-3_4645-2insG)
n.558+17_558+18insC
gnomAD v4
14g.23416314_23416315insCGGCCTCCTCCAGGGCTGACTGCAGCTCCATCTTCTCGGCCTCCAGCTGCTTTCCA613317655MHRT,MYH7c.4645-3_4645-2insGAAAGCAGCTGGAGGCCGAGAAGATGGAGCTGCAGTCAGCCCTGGAGGAGGCCG (n.4645-3_4645-2insGAAAGCAGCTGGAGGCCGAGAAGATGGAGCTGCAGTCAGCCCTGGAGGAGGCCG)
n.558+17_558+18insCGGCCTCCTCCAGGGCTGACTGCAGCTCCATCTTCTCGGCCTCCAGCTGCTTTC
dbSNP gnomAD v2
14g.23416315G>CCA257810783MHRT,MYH7c.4645-3C>G (n.4645-3C>G)
n.558+18G>C
dbSNP
14g.23416315G=CA2123466249MHRT,MYH7c.4645-3C= (n.4645-3C=)
n.558+18G=
14g.23416317delCA2499222574MHRT,MYH7c.4645-3del (n.4645-3del)
n.558+20del
ClinVar dbSNP
14g.23416316G>ACA2123466254MHRT,MYH7c.4645-4C>T (n.4645-4C>T)
n.558+19G>A
dbSNP gnomAD v4
14g.23416316G=CA2123466255MHRT,MYH7c.4645-4C= (n.4645-4C=)
n.558+19G=
14g.23416316_23416317insCCTCCTCCAGGGCTCA2624234791MHRT,MYH7c.4645-5_4645-4insAGCCCTGGAGGAGG (n.4645-5_4645-4insAGCCCTGGAGGAGG)
n.558+19_558+20insCCTCCTCCAGGGCT
gnomAD v4
14g.23416317G>ACA961068932MHRT,MYH7c.4645-5C>T (n.4645-5C>T)
n.558+20G>A
dbSNP gnomAD v3 gnomAD v4
14g.23416317G=CA2123466258MHRT,MYH7c.4645-5C= (n.4645-5C=)
n.558+20G=
14g.23416317_23416318delCA2575486692MHRT,MYH7c.4645-6_4645-5del (n.4645-6_4645-5del)
n.558+20_558+21del
14g.23416318_23416319insCTGCCA2624234796MHRT,MYH7c.4645-7_4645-6insGCAG (n.4645-7_4645-6insGCAG)
n.558+21_558+22insCTGC
gnomAD v4
14g.23416319A=CA2123466271MHRT,MYH7c.4645-7T= (n.4645-7T=)
n.558+22A=
14g.23416319A>CCA2800863162MHRT,MYH7c.4645-7T>G (n.4645-7T>G)
n.558+22A>C
14g.23416319A>GCA257810797MHRT,MYH7c.4645-7T>C (n.4645-7T>C)
n.558+22A>G
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23416319A>TCA2624234798MHRT,MYH7c.4645-7T>A (n.4645-7T>A)
n.558+22A>T
gnomAD v4
14g.23416319_23416320delinsAGCA2123466270MHRT,MYH7c.4645-8_4645-7delinsCT (n.4645-8_4645-7delinsCT)
n.558+22_558+23delinsAG
14g.23416320G>ACA2624234833MHRT,MYH7c.4645-8C>T (n.4645-8C>T)
n.558+23G>A
gnomAD v4
14g.23416323delCA043376MHRT,MYH7c.4645-8del (n.4645-8del)
n.558+26del
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23416321G>TCA2624234836MHRT,MYH7c.4645-9C>A (n.4645-9C>A)
n.558+24G>T
gnomAD v4
14g.23416322G>ACA2123466276MHRT,MYH7c.4645-10C>T (n.4645-10C>T)
n.558+25G>A
ClinVar dbSNP gnomAD v4
14g.23416322G=CA2123466279MHRT,MYH7c.4645-10C= (n.4645-10C=)
n.558+25G=
14g.23416322G>TCA2624234868MHRT,MYH7c.4645-10C>A (n.4645-10C>A)
n.558+25G>T
ClinVar gnomAD v4
14g.23416324T>ACA2123466282MHRT,MYH7c.4645-12A>T (n.4645-12A>T)
n.558+27T>A
dbSNP gnomAD v4
14g.23416324T=CA2123466283MHRT,MYH7c.4645-12A= (n.4645-12A=)
n.558+27T=
14g.23416325T>GCA961068940MHRT,MYH7c.4645-13A>C (n.4645-13A>C)
n.558+28T>G
dbSNP gnomAD v3 gnomAD v4
14g.23416325T=CA2123466284MHRT,MYH7c.4645-13A= (n.4645-13A=)
n.558+28T=
14g.23416326G>ACA613317657MHRT,MYH7c.4645-14C>T (n.4645-14C>T)
n.558+29G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23416326G=CA2123466286MHRT,MYH7c.4645-14C= (n.4645-14C=)
n.558+29G=
14g.23416330dupCA613317656MHRT,MYH7c.4645-14dup (n.4645-14dup)
n.558+33dup
dbSNP gnomAD v2 gnomAD v4
14g.23416330delCA2624234888MHRT,MYH7c.4645-14del (n.4645-14del)
n.558+33del
gnomAD v4
14g.23416327G>ACA043228MHRT,MYH7c.4645-15C>T (n.4645-15C>T)
n.558+30G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23416327G>CCA2123466298MHRT,MYH7c.4645-15C>G (n.4645-15C>G)
n.558+30G>C
ClinVar dbSNP gnomAD v4
14g.23416327G=CA2123466292MHRT,MYH7c.4645-15C= (n.4645-15C=)
n.558+30G=
14g.23416327G>TCA613317658MHRT,MYH7c.4645-15C>A (n.4645-15C>A)
n.558+30G>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23416328G>ACA043243MHRT,MYH7c.4645-16C>T (n.4645-16C>T)
n.558+31G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23416328G=CA2123466303MHRT,MYH7c.4645-16C= (n.4645-16C=)
n.558+31G=
14g.23416330_23416342delCA2624234907MHRT,MYH7c.4645-28_4645-16del (n.4645-28_4645-16del)
n.558+33_558+45del
gnomAD v4
14g.23416329G>ACA658798177MHRT,MYH7c.4645-17C>T (n.4645-17C>T)
n.558+32G>A
ClinVar dbSNP
14g.23416329G>CCA2624234915MHRT,MYH7c.4645-17C>G (n.4645-17C>G)
n.558+32G>C
gnomAD v4
14g.23416329G=CA2123466311MHRT,MYH7c.4645-17C= (n.4645-17C=)
n.558+32G=
14g.23416329G>TCA2624234916MHRT,MYH7c.4645-17C>A (n.4645-17C>A)
n.558+32G>T
gnomAD v4
14g.23416329_23416330insAACCCCA2800863169MHRT,MYH7c.4645-18_4645-17insGGGTT (n.4645-18_4645-17insGGGTT)
n.558+32_558+33insAACCC
14g.23416330G>ACA2624234920MHRT,MYH7c.4645-18C>T (n.4645-18C>T)
n.558+33G>A
ClinVar dbSNP gnomAD v4
14g.23416330G>TCA2580087887MHRT,MYH7c.4645-18C>A (n.4645-18C>A)
n.558+33G>T
ClinVar
14g.23416330_23416331insCGGCTATGCCCGTGACCATGGTCATCACA2800863171MHRT,MYH7c.4645-19_4645-18insTGATGACCATGGTCACGGGCATAGCCG (n.4645-19_4645-18insTGATGACCATGGTCACGGGCATAGCCG)
n.558+33_558+34insCGGCTATGCCCGTGACCATGGTCATCA
14g.23416331A=CA2123466317MHRT,MYH7c.4645-19T= (n.4645-19T=)
n.558+34A=
14g.23416331A>GCA613317659MHRT,MYH7c.4645-19T>C (n.4645-19T>C)
n.558+34A>G
dbSNP gnomAD v2 gnomAD v4
14g.23416332G>ACA2575486694MHRT,MYH7c.4645-20C>T (n.4645-20C>T)
n.558+35G>A
14g.23416334G>ACA043249MHRT,MYH7c.4645-22C>T (n.4645-22C>T)
n.558+37G>A
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23416334G=CA2123466323MHRT,MYH7c.4645-22C= (n.4645-22C=)
n.558+37G=
14g.23416334_23416335insCCA2800863172MHRT,MYH7c.4645-23_4645-22insG (n.4645-23_4645-22insG)
n.558+37_558+38insC
14g.23416335G>ACA2624234923MHRT,MYH7c.4645-23C>T (n.4645-23C>T)
n.558+38G>A
gnomAD v4
14g.23416335G=CA2123466325MHRT,MYH7c.4645-23C= (n.4645-23C=)
n.558+38G=
14g.23416335G>TCA2123466326MHRT,MYH7c.4645-23C>A (n.4645-23C>A)
n.558+38G>T
dbSNP
14g.23416336A=CA2123466328MHRT,MYH7c.4645-24T= (n.4645-24T=)
n.558+39A=
14g.23416336A>TCA043264MHRT,MYH7c.4645-24T>A (n.4645-24T>A)
n.558+39A>T
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23416336_23416337insCTACAAGCA2800863173MHRT,MYH7c.4645-25_4645-24insCTTGTAG (n.4645-25_4645-24insCTTGTAG)
n.558+39_558+40insCTACAAG
14g.23416337T>CCA043276MHRT,MYH7c.4645-25A>G (n.4645-25A>G)
n.558+40T>C
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23416337T>GCA2624234930MHRT,MYH7c.4645-25A>C (n.4645-25A>C)
n.558+40T>G
gnomAD v4
14g.23416337T=CA2123466333MHRT,MYH7c.4645-25A= (n.4645-25A=)
n.558+40T=
14g.23416338G>ACA2624234936MHRT,MYH7c.4645-26C>T (n.4645-26C>T)
n.558+41G>A
gnomAD v4
14g.23416338G=CA2123466337MHRT,MYH7c.4645-26C= (n.4645-26C=)
n.558+41G=
14g.23416338G>TCA043282MHRT,MYH7c.4645-26C>A (n.4645-26C>A)
n.558+41G>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23416339C>ACA2624234939MHRT,MYH7c.4645-27G>T (n.4645-27G>T)
n.558+42C>A
gnomAD v4
14g.23416339C=CA2123466339MHRT,MYH7c.4645-27G= (n.4645-27G=)
n.558+42C=
14g.23416339C>TCA043302MHRT,MYH7c.4645-27G>A (n.4645-27G>A)
n.558+42C>T
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23416339_23416340insGCCTCGATTGCGGCTGCCTCTGTGGTGGCGACA2800863175MHRT,MYH7c.4645-28_4645-27insTCGCCACCACAGAGGCAGCCGCAATCGAGGC (n.4645-28_4645-27insTCGCCACCACAGAGGCAGCCGCAATCGAGGC)
n.558+42_558+43insGCCTCGATTGCGGCTGCCTCTGTGGTGGCGA
14g.23416340A>CCA2575486697MHRT,MYH7c.4645-28T>G (n.4645-28T>G)
n.558+43A>C
14g.23416340A>GCA2624234951MHRT,MYH7c.4645-28T>C (n.4645-28T>C)
n.558+43A>G
gnomAD v4
14g.23416341G>ACA613317660MHRT,MYH7c.4645-29C>T (n.4645-29C>T)
n.558+44G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23416341G=CA2123466344MHRT,MYH7c.4645-29C= (n.4645-29C=)
n.558+44G=
14g.23416342delCA2624234957MHRT,MYH7c.4645-29del (n.4645-29del)
n.558+45del
gnomAD v4
14g.23416343C>ACA2624234960MHRT,MYH7c.4645-31G>T (n.4645-31G>T)
n.558+46C>A
gnomAD v4
14g.23416343C>TCA2624234979MHRT,MYH7c.4645-31G>A (n.4645-31G>A)
n.558+46C>T
gnomAD v4
14g.23416344A=CA2123466347MHRT,MYH7c.4645-32T= (n.4645-32T=)
n.558+47A=
14g.23416344A>GCA2123466348MHRT,MYH7c.4645-32T>C (n.4645-32T>C)
n.558+47A>G
dbSNP
14g.23416345G=CA2123466351MHRT,MYH7c.4645-33C= (n.4645-33C=)
n.558+48G=
14g.23416345G>TCA613317661MHRT,MYH7c.4645-33C>A (n.4645-33C>A)
n.558+48G>T
dbSNP gnomAD v2 gnomAD v4
14g.23416346A=CA2123466352MHRT,MYH7c.4645-34T= (n.4645-34T=)
n.558+49A=
14g.23416346A>GCA613317662MHRT,MYH7c.4645-34T>C (n.4645-34T>C)
n.558+49A>G
dbSNP gnomAD v2 gnomAD v4
14g.23416346_23416350delinsACAGTCA2123466354MHRT,MYH7c.4645-38_4645-34delinsACTGT (n.4645-38_4645-34delinsACTGT)
n.558+49_558+53delinsACAGT
14g.23416347C>ACA2624235018MHRT,MYH7c.4645-35G>T (n.4645-35G>T)
n.558+50C>A
gnomAD v4
14g.23416347C>GCA2624235017MHRT,MYH7c.4645-35G>C (n.4645-35G>C)
n.558+50C>G
gnomAD v4
14g.23416347C>TCA2575486698MHRT,MYH7c.4645-35G>A (n.4645-35G>A)
n.558+50C>T
14g.23416350_23416353delCA043321MHRT,MYH7c.4645-38_4645-35del (n.4645-38_4645-35del)
n.558+53_558+56del
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23416349G>CCA2575486699MHRT,MYH7c.4645-37C>G (n.4645-37C>G)
n.558+52G>C
gnomAD v4
14g.23416350T>CCA043327MHRT,MYH7c.4645-38A>G (n.4645-38A>G)
n.558+53T>C
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23416350T=CA2123466358MHRT,MYH7c.4645-38A= (n.4645-38A=)
n.558+53T=

Number of alleles fetched