Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23419529A=CA2123445231MYH7c.3807T= (p.Ser1269=)
14g.23419529A>CCA485620490MYH7c.3807T>G (p.Ser1269=)
14g.23419529A>GCA485620491MYH7c.3807T>C (p.Ser1269=)
ClinVar dbSNP
14g.23419529A>TCA485620494MYH7c.3807T>A (p.Ser1269=)
14g.23419530G>ACA389042021MYH7c.3806C>T (p.Ser1269Phe)
14g.23419530G>CCA389042022MYH7c.3806C>G (p.Ser1269Cys)
14g.23419530G>TCA389042023MYH7c.3806C>A (p.Ser1269Tyr)
14g.23419531A>CCA389042025MYH7c.3805T>G (p.Ser1269Ala)
14g.23419531A>GCA389042027MYH7c.3805T>C (p.Ser1269Pro)
14g.23419531A>TCA389042028MYH7c.3805T>A (p.Ser1269Thr)
14g.23419532A=CA2123445240MYH7c.3804T= (p.Arg1268=)
14g.23419532A>CCA485620507MYH7c.3804T>G (p.Arg1268=)
14g.23419532A>GCA485620503MYH7c.3804T>C (p.Arg1268=)
ClinVar dbSNP gnomAD v4
14g.23419532A>TCA485620505MYH7c.3804T>A (p.Arg1268=)
14g.23419533C>ACA389042030MYH7c.3803G>T (p.Arg1268Leu)
14g.23419533C=CA2123445249MYH7c.3803G= (p.Arg1268=)
14g.23419533C>GCA014107MYH7c.3803G>C (p.Arg1268Pro)
ClinVar dbSNP
14g.23419533C>TCA014102MYH7c.3803G>A (p.Arg1268His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419534G>ACA389042033MYH7c.3802C>T (p.Arg1268Cys)
ClinVar dbSNP gnomAD v4 COSMIC
14g.23419534G>CCA389042034MYH7c.3802C>G (p.Arg1268Gly)
14g.23419534G=CA2123445265MYH7c.3802C= (p.Arg1268=)
14g.23419534G>TCA389042035MYH7c.3802C>A (p.Arg1268Ser)
gnomAD v4
14g.23419535C>ACA389042037MYH7c.3801G>T (p.Gln1267His)
14g.23419535C=CA2123445278MYH7c.3801G= (p.Gln1267=)
14g.23419535C>GCA038976MYH7c.3801G>C (p.Gln1267His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419535C>TCA16606534MYH7c.3801G>A (p.Gln1267=)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23419536T>ACA389042042MYH7c.3800A>T (p.Gln1267Leu)
14g.23419536T>CCA389042041MYH7c.3800A>G (p.Gln1267Arg)
14g.23419536T>GCA389042040MYH7c.3800A>C (p.Gln1267Pro)
14g.23419537G>ACA389042043MYH7c.3799C>T (p.Gln1267Ter)
ClinVar dbSNP
14g.23419537G>CCA389042045MYH7c.3799C>G (p.Gln1267Glu)
14g.23419537G>TCA389042047MYH7c.3799C>A (p.Gln1267Lys)
14g.23419538G>ACA485620523MYH7c.3798C>T (p.Thr1266=)
gnomAD v4
14g.23419538G>CCA485620524MYH7c.3798C>G (p.Thr1266=)
ClinVar
14g.23419538G=CA2123445282MYH7c.3798C= (p.Thr1266=)
14g.23419538G>TCA485620526MYH7c.3798C>A (p.Thr1266=)
dbSNP
14g.23419539G>ACA389042049MYH7c.3797C>T (p.Thr1266Ile)
ClinVar
14g.23419539G>CCA389042050MYH7c.3797C>G (p.Thr1266Ser)
ClinVar dbSNP gnomAD v4
14g.23419539G=CA2123445288MYH7c.3797C= (p.Thr1266=)
14g.23419539G>TCA038945MYH7c.3797C>A (p.Thr1266Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419540T>ACA389042051MYH7c.3796A>T (p.Thr1266Ser)
14g.23419540T>CCA389042054MYH7c.3796A>G (p.Thr1266Ala)
gnomAD v4
14g.23419540T>GCA389042053MYH7c.3796A>C (p.Thr1266Pro)
dbSNP
14g.23419540T=CA2123445294MYH7c.3796A= (p.Thr1266=)
14g.23419541C>ACA389042056MYH7c.3795G>T (p.Glu1265Asp)
14g.23419541C>GCA389042057MYH7c.3795G>C (p.Glu1265Asp)
14g.23419541C>TCA485620532MYH7c.3795G>A (p.Glu1265=)
ClinVar dbSNP
14g.23419542T>ACA389042058MYH7c.3794A>T (p.Glu1265Val)
14g.23419542T>CCA389042060MYH7c.3794A>G (p.Glu1265Gly)
14g.23419542T>GCA389042062MYH7c.3794A>C (p.Glu1265Ala)
14g.23419543C>ACA389042064MYH7c.3793G>T (p.Glu1265Ter)
14g.23419543C>GCA389042065MYH7c.3793G>C (p.Glu1265Gln)
14g.23419543C>TCA389042066MYH7c.3793G>A (p.Glu1265Lys)
COSMIC
14g.23419544C>ACA389042068MYH7c.3792G>T (p.Glu1264Asp)
14g.23419544C>GCA389042070MYH7c.3792G>C (p.Glu1264Asp)
14g.23419544C>TCA485620538MYH7c.3792G>A (p.Glu1264=)
14g.23419545T>ACA389042072MYH7c.3791A>T (p.Glu1264Val)
14g.23419545T>CCA389042073MYH7c.3791A>G (p.Glu1264Gly)
14g.23419545T>GCA389042074MYH7c.3791A>C (p.Glu1264Ala)
14g.23419546C>ACA389042078MYH7c.3790G>T (p.Glu1264Ter)
14g.23419546C>GCA389042080MYH7c.3790G>C (p.Glu1264Gln)
14g.23419546C>TCA389042076MYH7c.3790G>A (p.Glu1264Lys)
14g.23419547delCA2573149837MYH7c.3790del (p.Glu1264ArgfsTer?)
ClinVar dbSNP
14g.23419547C>ACA038913MYH7c.3789G>T (p.Ala1263=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419547C=CA2123445304MYH7c.3789G= (p.Ala1263=)
14g.23419547C>GCA038905MYH7c.3789G>C (p.Ala1263=)
dbSNP ExAC gnomAD v2
14g.23419547C>TCA038883MYH7c.3789G>A (p.Ala1263=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23419548G>ACA389042619MYH7c.3788C>T (p.Ala1263Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23419548G>CCA389042621MYH7c.3788C>G (p.Ala1263Gly)
14g.23419548G=CA2123445325MYH7c.3788C= (p.Ala1263=)
14g.23419548G>TCA038858MYH7c.3788C>A (p.Ala1263Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419549C>ACA389042626MYH7c.3787G>T (p.Ala1263Ser)
14g.23419549C=CA2123445331MYH7c.3787G= (p.Ala1263=)
14g.23419549C>GCA389042624MYH7c.3787G>C (p.Ala1263Pro)
14g.23419549C>TCA389042623MYH7c.3787G>A (p.Ala1263Thr)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23419550C>ACA389042628MYH7c.3786G>T (p.Lys1262Asn)
14g.23419550C=CA2123445339MYH7c.3786G= (p.Lys1262=)
14g.23419550C>GCA389042630MYH7c.3786G>C (p.Lys1262Asn)
14g.23419550C>TCA257815010MYH7c.3786G>A (p.Lys1262=)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23419551T>ACA389042631MYH7c.3785A>T (p.Lys1262Met)
14g.23419551T>CCA389042633MYH7c.3785A>G (p.Lys1262Arg)
14g.23419551T>GCA389042635MYH7c.3785A>C (p.Lys1262Thr)
14g.23419552T>ACA389042639MYH7c.3784A>T (p.Lys1262Ter)
14g.23419552T>CCA389042636MYH7c.3784A>G (p.Lys1262Glu)
gnomAD v4
14g.23419552T>GCA389042637MYH7c.3784A>C (p.Lys1262Gln)
14g.23419553G>ACA485766377MYH7c.3783C>T (p.Ser1261=)
gnomAD v4
14g.23419553G>CCA389042641MYH7c.3783C>G (p.Ser1261Arg)
ClinVar dbSNP
14g.23419553G=CA2123445347MYH7c.3783C= (p.Ser1261=)
14g.23419553G>TCA389042643MYH7c.3783C>A (p.Ser1261Arg)
14g.23419554C>ACA389042644MYH7c.3782G>T (p.Ser1261Ile)
14g.23419554C=CA2123445352MYH7c.3782G= (p.Ser1261=)
14g.23419554C>GCA389042645MYH7c.3782G>C (p.Ser1261Thr)
gnomAD v4
14g.23419554C>TCA038835MYH7c.3782G>A (p.Ser1261Asn)
dbSNP ExAC gnomAD v2 COSMIC
14g.23419555T>ACA389042648MYH7c.3781A>T (p.Ser1261Cys)
14g.23419555T>CCA389042649MYH7c.3781A>G (p.Ser1261Gly)
14g.23419555T>GCA014093MYH7c.3781A>C (p.Ser1261Arg)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23419555T=CA2123445358MYH7c.3781A= (p.Ser1261=)
14g.23419556C>ACA485766382MYH7c.3780G>T (p.Arg1260=)
14g.23419556C>GCA485766383MYH7c.3780G>C (p.Arg1260=)
14g.23419556C>TCA485766384MYH7c.3780G>A (p.Arg1260=)
14g.23419557C>ACA389042651MYH7c.3779G>T (p.Arg1260Leu)
gnomAD v4
14g.23419557C=CA2123445368MYH7c.3779G= (p.Arg1260=)
14g.23419557C>GCA014087MYH7c.3779G>C (p.Arg1260Pro)
ClinVar dbSNP
14g.23419557C>TCA038820MYH7c.3779G>A (p.Arg1260Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419558G>ACA038804MYH7c.3778C>T (p.Arg1260Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23419558G>CCA389042654MYH7c.3778C>G (p.Arg1260Gly)
ClinVar gnomAD v4
14g.23419558G=CA2123445378MYH7c.3778C= (p.Arg1260=)
14g.23419558G>TCA485766386MYH7c.3778C>A (p.Arg1260=)
14g.23419559G>ACA014078MYH7c.3777C>T (p.His1259=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419559G>CCA389042657MYH7c.3777C>G (p.His1259Gln)
14g.23419559G=CA2123445385MYH7c.3777C= (p.His1259=)
14g.23419559G>TCA038769MYH7c.3777C>A (p.His1259Gln)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419560T>ACA389042659MYH7c.3776A>T (p.His1259Leu)
14g.23419560T>CCA389042660MYH7c.3776A>G (p.His1259Arg)
14g.23419560T>GCA389042662MYH7c.3776A>C (p.His1259Pro)
14g.23419561G>ACA389042664MYH7c.3775C>T (p.His1259Tyr)
14g.23419561G>CCA389042666MYH7c.3775C>G (p.His1259Asp)
14g.23419561G>TCA389042667MYH7c.3775C>A (p.His1259Asn)
14g.23419562C>ACA389042669MYH7c.3774G>T (p.Glu1258Asp)
14g.23419562C=CA2123445394MYH7c.3774G= (p.Glu1258=)
14g.23419562C>GCA389042670MYH7c.3774G>C (p.Glu1258Asp)
14g.23419562C>TCA257815058MYH7c.3774G>A (p.Glu1258=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23419563T>ACA389042673MYH7c.3773A>T (p.Glu1258Val)
14g.23419563T>CCA389042674MYH7c.3773A>G (p.Glu1258Gly)
14g.23419563T>GCA389042675MYH7c.3773A>C (p.Glu1258Ala)
gnomAD v4
14g.23419564C>ACA389042679MYH7c.3772G>T (p.Glu1258Ter)
14g.23419564C=CA2123445416MYH7c.3772G= (p.Glu1258=)
14g.23419564C>GCA389042680MYH7c.3772G>C (p.Glu1258Gln)
14g.23419564C>TCA389042678MYH7c.3772G>A (p.Glu1258Lys)
14g.23419565A=CA2123445424MYH7c.3771T= (p.Asn1257=)
14g.23419565A>CCA389042683MYH7c.3771T>G (p.Asn1257Lys)
14g.23419565A>GCA014068MYH7c.3771T>C (p.Asn1257=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419565A>TCA389042685MYH7c.3771T>A (p.Asn1257Lys)
14g.23419565dupCA7116299MYH7c.3771dup (p.Glu1258Ter)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419566T>ACA389042689MYH7c.3770A>T (p.Asn1257Ile)
14g.23419566T>CCA014062MYH7c.3770A>G (p.Asn1257Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419566T>GCA389042687MYH7c.3770A>C (p.Asn1257Thr)
14g.23419566T=CA2123445432MYH7c.3770A= (p.Asn1257=)
14g.23419567T>ACA389042691MYH7c.3769A>T (p.Asn1257Tyr)
14g.23419567T>CCA389042692MYH7c.3769A>G (p.Asn1257Asp)
14g.23419567T>GCA389042693MYH7c.3769A>C (p.Asn1257His)
ClinVar dbSNP gnomAD v4
14g.23419567T=CA2123445439MYH7c.3769A= (p.Asn1257=)
14g.23419568C>ACA389042694MYH7c.3768G>T (p.Met1256Ile)
14g.23419568C>GCA389042695MYH7c.3768G>C (p.Met1256Ile)
14g.23419568C>TCA389042697MYH7c.3768G>A (p.Met1256Ile)
COSMIC
14g.23419569A=CA2123445444MYH7c.3767T= (p.Met1256=)
14g.23419569A>CCA389042699MYH7c.3767T>G (p.Met1256Arg)
14g.23419569A>GCA389042702MYH7c.3767T>C (p.Met1256Thr)
ClinVar dbSNP
14g.23419569A>TCA389042701MYH7c.3767T>A (p.Met1256Lys)
14g.23419570T>ACA389042703MYH7c.3766A>T (p.Met1256Leu)
14g.23419570T>CCA389042706MYH7c.3766A>G (p.Met1256Val)
14g.23419570T>GCA389042705MYH7c.3766A>C (p.Met1256Leu)
14g.23419571C>ACA389042708MYH7c.3765G>T (p.Gln1255His)
gnomAD v4
14g.23419571C>GCA389042710MYH7c.3765G>C (p.Gln1255His)
14g.23419571C>TCA485766402MYH7c.3765G>A (p.Gln1255=)
14g.23419572T>ACA389042711MYH7c.3764A>T (p.Gln1255Leu)
14g.23419572T>CCA389042712MYH7c.3764A>G (p.Gln1255Arg)
14g.23419572T>GCA389042714MYH7c.3764A>C (p.Gln1255Pro)
14g.23419573G>ACA389042716MYH7c.3763C>T (p.Gln1255Ter)
dbSNP
14g.23419573G>CCA389042718MYH7c.3763C>G (p.Gln1255Glu)
14g.23419573G=CA2123445450MYH7c.3763C= (p.Gln1255=)
14g.23419573G>TCA389042719MYH7c.3763C>A (p.Gln1255Lys)
14g.23419574G>ACA485766405MYH7c.3762C>T (p.Asp1254=)
ClinVar gnomAD v4
14g.23419574G>CCA389042720MYH7c.3762C>G (p.Asp1254Glu)
14g.23419574G>TCA389042722MYH7c.3762C>A (p.Asp1254Glu)
14g.23419575T>ACA389042724MYH7c.3761A>T (p.Asp1254Val)
14g.23419575T>CCA389042726MYH7c.3761A>G (p.Asp1254Gly)
14g.23419575T>GCA389042727MYH7c.3761A>C (p.Asp1254Ala)
14g.23419576C>ACA389042729MYH7c.3760G>T (p.Asp1254Tyr)
14g.23419576C>GCA389042732MYH7c.3760G>C (p.Asp1254His)
14g.23419576C>TCA389042730MYH7c.3760G>A (p.Asp1254Asn)
gnomAD v4
14g.23419577T>ACA389042734MYH7c.3759A>T (p.Glu1253Asp)
14g.23419577T>CCA485766409MYH7c.3759A>G (p.Glu1253=)
dbSNP
14g.23419577T>GCA389042735MYH7c.3759A>C (p.Glu1253Asp)
gnomAD v4
14g.23419577T=CA2123445455MYH7c.3759A= (p.Glu1253=)
14g.23419578T>ACA389042736MYH7c.3758A>T (p.Glu1253Val)
14g.23419578T>CCA389042738MYH7c.3758A>G (p.Glu1253Gly)
14g.23419578T>GCA389042740MYH7c.3758A>C (p.Glu1253Ala)
14g.23419578T=CA2123445457MYH7c.3758A= (p.Glu1253=)
14g.23419579C>ACA389042742MYH7c.3757G>T (p.Glu1253Ter)
14g.23419579C>GCA389042743MYH7c.3757G>C (p.Glu1253Gln)
14g.23419579C>TCA389042744MYH7c.3757G>A (p.Glu1253Lys)
14g.23419579_23419580dupCA2123445458MYH7c.3756_3757dup (p.Glu1253GlyfsTer5)
dbSNP
14g.23419580C>ACA389042746MYH7c.3756G>T (p.Leu1252Phe)
14g.23419580C>GCA389042748MYH7c.3756G>C (p.Leu1252Phe)
14g.23419580C>TCA485766411MYH7c.3756G>A (p.Leu1252=)
14g.23419581A=CA2123445462MYH7c.3755T= (p.Leu1252=)
14g.23419581A>CCA389042752MYH7c.3755T>G (p.Leu1252Trp)
ClinVar
14g.23419581A>GCA389042751MYH7c.3755T>C (p.Leu1252Ser)
dbSNP gnomAD v2 gnomAD v4
14g.23419581A>TCA389042750MYH7c.3755T>A (p.Leu1252Ter)
14g.23419582A=CA2123445467MYH7c.3754T= (p.Leu1252=)
14g.23419582A>CCA389042754MYH7c.3754T>G (p.Leu1252Val)
14g.23419582A>GCA014051MYH7c.3754T>C (p.Leu1252=)
ClinVar dbSNP gnomAD v4
14g.23419582A>TCA389042756MYH7c.3754T>A (p.Leu1252Met)
14g.23419583G>ACA038728MYH7c.3753C>T (p.Thr1251=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419583G>CCA485766414MYH7c.3753C>G (p.Thr1251=)
ClinVar dbSNP gnomAD v4
14g.23419583G=CA2123445473MYH7c.3753C= (p.Thr1251=)
14g.23419583G>TCA485766415MYH7c.3753C>A (p.Thr1251=)
14g.23419584G>ACA389042758MYH7c.3752C>T (p.Thr1251Ile)
ClinVar dbSNP
14g.23419584G>CCA389042760MYH7c.3752C>G (p.Thr1251Ser)
14g.23419584G=CA2123445480MYH7c.3752C= (p.Thr1251=)
14g.23419584G>TCA389042761MYH7c.3752C>A (p.Thr1251Asn)
14g.23419585T>ACA389042763MYH7c.3751A>T (p.Thr1251Ser)
14g.23419585T>CCA389042764MYH7c.3751A>G (p.Thr1251Ala)
14g.23419585T>GCA389042766MYH7c.3751A>C (p.Thr1251Pro)
14g.23419586C>ACA485766426MYH7c.3750G>T (p.Arg1250=)
ClinVar
14g.23419586C=CA2123445485MYH7c.3750G= (p.Arg1250=)
14g.23419586C>GCA485766429MYH7c.3750G>C (p.Arg1250=)
14g.23419586C>TCA038721MYH7c.3750G>A (p.Arg1250=)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419587delCA2624230713MYH7c.3750del (p.Thr1251ProfsTer6)
gnomAD v4
14g.23419587C>ACA389042767MYH7c.3749G>T (p.Arg1250Leu)
14g.23419587C=CA2123445488MYH7c.3749G= (p.Arg1250=)
14g.23419587C>GCA014046MYH7c.3749G>C (p.Arg1250Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419587C>TCA038693MYH7c.3749G>A (p.Arg1250Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23419588G>ACA014039MYH7c.3748C>T (p.Arg1250Trp)
ClinVar dbSNP gnomAD v4
14g.23419588G>CCA389042770MYH7c.3748C>G (p.Arg1250Gly)
ClinVar dbSNP gnomAD v4
14g.23419588G=CA2123445499MYH7c.3748C= (p.Arg1250=)
14g.23419588G>TCA485766431MYH7c.3748C>A (p.Arg1250=)
14g.23419589delCA2825002214MYH7c.3748del (p.Arg1250GlyfsTer7)
ClinVar
14g.23419589G>ACA485766432MYH7c.3747C>T (p.Cys1249=)
14g.23419589G>CCA389042772MYH7c.3747C>G (p.Cys1249Trp)
gnomAD v4
14g.23419589G>TCA389042774MYH7c.3747C>A (p.Cys1249Ter)
14g.23419590C>ACA389042775MYH7c.3746G>T (p.Cys1249Phe)
14g.23419590C>GCA389042777MYH7c.3746G>C (p.Cys1249Ser)
14g.23419590C>TCA389042778MYH7c.3746G>A (p.Cys1249Tyr)
ClinVar
14g.23419592_23419593delCA2697553856MYH7c.3745_3746del (p.Cys1249ProfsTer9)
ClinVar
14g.23419591A>CCA389042779MYH7c.3745T>G (p.Cys1249Gly)
14g.23419591A>GCA389042781MYH7c.3745T>C (p.Cys1249Arg)
gnomAD v4
14g.23419591A>TCA389042782MYH7c.3745T>A (p.Cys1249Ser)
14g.23419592C>ACA389042783MYH7c.3744G>T (p.Met1248Ile)
14g.23419592C>GCA389042784MYH7c.3744G>C (p.Met1248Ile)
14g.23419592C>TCA389042786MYH7c.3744G>A (p.Met1248Ile)
14g.23419593A=CA2123445519MYH7c.3743T= (p.Met1248=)
14g.23419593A>CCA389042788MYH7c.3743T>G (p.Met1248Arg)
gnomAD v4
14g.23419593A>GCA389042790MYH7c.3743T>C (p.Met1248Thr)
14g.23419593A>TCA16614479MYH7c.3743T>A (p.Met1248Lys)
ClinVar dbSNP gnomAD v4
14g.23419594T>ACA389042791MYH7c.3742A>T (p.Met1248Leu)
14g.23419594T>CCA389042795MYH7c.3742A>G (p.Met1248Val)
14g.23419594T>GCA389042793MYH7c.3742A>C (p.Met1248Leu)
gnomAD v4
14g.23419595C>ACA389042797MYH7c.3741G>T (p.Lys1247Asn)
14g.23419595C>GCA389042798MYH7c.3741G>C (p.Lys1247Asn)
14g.23419595C>TCA485766438MYH7c.3741G>A (p.Lys1247=)
14g.23419595_23419596delinsCTCA2123445522MYH7c.3740_3741delinsAG (p.Lys1247=)
14g.23419596T>ACA389042800MYH7c.3740A>T (p.Lys1247Met)
ClinVar
14g.23419596T>CCA389042801MYH7c.3740A>G (p.Lys1247Arg)
14g.23419596T>GCA389042803MYH7c.3740A>C (p.Lys1247Thr)
14g.23419597delCA613317671MYH7c.3740del (p.Lys1247ArgfsTer10)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23419597T>ACA389042805MYH7c.3739A>T (p.Lys1247Ter)
14g.23419597T>CCA389042806MYH7c.3739A>G (p.Lys1247Glu)
gnomAD v4
14g.23419597T>GCA389042807MYH7c.3739A>C (p.Lys1247Gln)
14g.23419598C>ACA389042811MYH7c.3738G>T (p.Glu1246Asp)
14g.23419598C=CA2123445529MYH7c.3738G= (p.Glu1246=)
14g.23419598C>GCA389042809MYH7c.3738G>C (p.Glu1246Asp)
14g.23419598C>TCA485766443MYH7c.3738G>A (p.Glu1246=)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23419599T>ACA389042812MYH7c.3737A>T (p.Glu1246Val)
14g.23419599T>CCA389042813MYH7c.3737A>G (p.Glu1246Gly)
14g.23419599T>GCA389042814MYH7c.3737A>C (p.Glu1246Ala)
14g.23419600C>ACA389042817MYH7c.3736G>T (p.Glu1246Ter)
14g.23419600C>GCA389042819MYH7c.3736G>C (p.Glu1246Gln)
14g.23419600C>TCA389042820MYH7c.3736G>A (p.Glu1246Lys)
14g.23419601C>ACA485766446MYH7c.3735G>T (p.Leu1245=)
14g.23419601C>GCA485766445MYH7c.3735G>C (p.Leu1245=)
14g.23419601C>TCA485766447MYH7c.3735G>A (p.Leu1245=)
14g.23419602A=CA2123445534MYH7c.3734T= (p.Leu1245=)
14g.23419602A>CCA389042825MYH7c.3734T>G (p.Leu1245Arg)
14g.23419602A>GCA389042822MYH7c.3734T>C (p.Leu1245Pro)
COSMIC
14g.23419602A>TCA014012MYH7c.3734T>A (p.Leu1245Gln)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23419603G>ACA485766449MYH7c.3733C>T (p.Leu1245=)
14g.23419603G>CCA389042826MYH7c.3733C>G (p.Leu1245Val)
14g.23419603G>TCA389042827MYH7c.3733C>A (p.Leu1245Met)
14g.23419604G>ACA485766452MYH7c.3732C>T (p.Asn1244=)
14g.23419604G>CCA389042829MYH7c.3732C>G (p.Asn1244Lys)
14g.23419604G>TCA389042830MYH7c.3732C>A (p.Asn1244Lys)
ClinVar
14g.23419605T>ACA389042833MYH7c.3731A>T (p.Asn1244Ile)
14g.23419605T>CCA389042834MYH7c.3731A>G (p.Asn1244Ser)
14g.23419605T>GCA389042835MYH7c.3731A>C (p.Asn1244Thr)
14g.23419606T>ACA389042837MYH7c.3730A>T (p.Asn1244Tyr)
14g.23419606T>CCA389042838MYH7c.3730A>G (p.Asn1244Asp)
ClinVar dbSNP
14g.23419606T>GCA014003MYH7c.3730A>C (p.Asn1244His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419606T=CA2123445542MYH7c.3730A= (p.Asn1244=)
14g.23419607A=CA2123445549MYH7c.3729T= (p.Ala1243=)
14g.23419607A>CCA485766454MYH7c.3729T>G (p.Ala1243=)
dbSNP
14g.23419607A>GCA485766455MYH7c.3729T>C (p.Ala1243=)
dbSNP
14g.23419607A>TCA485766456MYH7c.3729T>A (p.Ala1243=)
14g.23419608G>ACA389042841MYH7c.3728C>T (p.Ala1243Val)
14g.23419608G>CCA389042842MYH7c.3728C>G (p.Ala1243Gly)
ClinVar
14g.23419608G>TCA389042844MYH7c.3728C>A (p.Ala1243Asp)
14g.23419609C>ACA389042846MYH7c.3727G>T (p.Ala1243Ser)
14g.23419609C>GCA389042848MYH7c.3727G>C (p.Ala1243Pro)
14g.23419609C>TCA389042847MYH7c.3727G>A (p.Ala1243Thr)
14g.23419610C>ACA389042850MYH7c.3727-1G>T (n.3727-1G>T)
14g.23419610C>GCA389042851MYH7c.3727-1G>C (n.3727-1G>C)
14g.23419610C>TCA389042853MYH7c.3727-1G>A (n.3727-1G>A)
14g.23419611T>ACA389042854MYH7c.3727-2A>T (n.3727-2A>T)
14g.23419611T>CCA389042855MYH7c.3727-2A>G (n.3727-2A>G)
14g.23419611T>GCA389042856MYH7c.3727-2A>C (n.3727-2A>C)
dbSNP gnomAD v3 gnomAD v4
14g.23419611T=CA2123445553MYH7c.3727-2A= (n.3727-2A=)
14g.23419612G>ACA2624230768MYH7c.3727-3C>T (n.3727-3C>T)
gnomAD v4
14g.23419612G>CCA257815098MYH7c.3727-3C>G (n.3727-3C>G)
dbSNP
14g.23419612G=CA2123445554MYH7c.3727-3C= (n.3727-3C=)
14g.23419612G>TCA257815096MYH7c.3727-3C>A (n.3727-3C>A)
dbSNP
14g.23419613A>CCA2573149838MYH7c.3727-4T>G (n.3727-4T>G)
ClinVar dbSNP
14g.23419614G>ACA2123445563MYH7c.3727-5C>T (n.3727-5C>T)
ClinVar dbSNP gnomAD v4
14g.23419614G>CCA961071298MYH7c.3727-5C>G (n.3727-5C>G)
dbSNP gnomAD v3 gnomAD v4
14g.23419614G=CA2123445559MYH7c.3727-5C= (n.3727-5C=)
14g.23419614G>TCA704287811MYH7c.3727-5C>A (n.3727-5C>A)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23419616A>GCA2575504258MYH7c.3727-7T>C (n.3727-7T>C)
14g.23419616A>TCA2624230779MYH7c.3727-7T>A (n.3727-7T>A)
gnomAD v4
14g.23419617G>ACA2123445570MYH7c.3727-8C>T (n.3727-8C>T)
ClinVar dbSNP gnomAD v4
14g.23419617G=CA2123445569MYH7c.3727-8C= (n.3727-8C=)
14g.23419618G>ACA2800863598MYH7c.3727-9C>T (n.3727-9C>T)
14g.23419620A=CA2123445572MYH7c.3727-11T= (n.3727-11T=)
14g.23419620A>GCA038596MYH7c.3727-11T>C (n.3727-11T>C)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419621A>TCA2590018540MYH7c.3727-12T>A (n.3727-12T>A)
dbSNP gnomAD v3 gnomAD v4
14g.23419622G>ACA2624230791MYH7c.3727-13C>T (n.3727-13C>T)
gnomAD v4
14g.23419624A=CA2123445576MYH7c.3727-15T= (n.3727-15T=)
14g.23419624A>GCA2825002215MYH7c.3727-15T>C (n.3727-15T>C)
ClinVar
14g.23419624A>TCA2123445577MYH7c.3727-15T>A (n.3727-15T>A)
ClinVar dbSNP gnomAD v4
14g.23419626A=CA2123445580MYH7c.3727-17T= (n.3727-17T=)
14g.23419626A>GCA613317672MYH7c.3727-17T>C (n.3727-17T>C)
dbSNP gnomAD v2 gnomAD v4
14g.23419626A>TCA2575504259MYH7c.3727-17T>A (n.3727-17T>A)
gnomAD v4
14g.23419627G>ACA038602MYH7c.3727-18C>T (n.3727-18C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419627G=CA2123445584MYH7c.3727-18C= (n.3727-18C=)
14g.23419627G>TCA2624230796MYH7c.3727-18C>A (n.3727-18C>A)
gnomAD v4

Number of alleles fetched