Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23415756C>ACA389037104MHRT,MYH7c.5030G>T (p.Arg1677Leu)
n.188C>A
gnomAD v4
14g.23415756C=CA2123464308MHRT,MYH7c.5030G= (p.Arg1677=)
n.188C=
14g.23415756C>GCA389037105MHRT,MYH7c.5030G>C (p.Arg1677Pro)
n.188C>G
ClinVar
14g.23415756C>TCA015595MHRT,MYH7c.5030G>A (p.Arg1677His)
n.188C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23415757G>ACA015584MHRT,MYH7c.5029C>T (p.Arg1677Cys)
n.189G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23415757G>CCA389037106MHRT,MYH7c.5029C>G (p.Arg1677Gly)
n.189G>C
14g.23415757G=CA2123464318MHRT,MYH7c.5029C= (p.Arg1677=)
n.189G=
14g.23415757G>TCA389037107MHRT,MYH7c.5029C>A (p.Arg1677Ser)
n.189G>T
14g.23415758C>ACA485766208MHRT,MYH7c.5028G>T (p.Arg1676=)
n.190C>A
14g.23415758C>GCA485766209MHRT,MYH7c.5028G>C (p.Arg1676=)
n.190C>G
14g.23415758C>TCA485766210MHRT,MYH7c.5028G>A (p.Arg1676=)
n.190C>T
14g.23415759C>ACA389037110MHRT,MYH7c.5027G>T (p.Arg1676Leu)
n.191C>A
14g.23415759C=CA2123464324MHRT,MYH7c.5027G= (p.Arg1676=)
n.191C=
14g.23415759C>GCA389037109MHRT,MYH7c.5027G>C (p.Arg1676Pro)
n.191C>G
14g.23415759C>TCA389037108MHRT,MYH7c.5027G>A (p.Arg1676Gln)
n.191C>T
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23415760G>ACA044958MHRT,MYH7c.5026C>T (p.Arg1676Trp)
n.192G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23415760G>CCA389037111MHRT,MYH7c.5026C>G (p.Arg1676Gly)
n.192G>C
14g.23415760G=CA2123464332MHRT,MYH7c.5026C= (p.Arg1676=)
n.192G=
14g.23415760G>TCA485766217MHRT,MYH7c.5026C>A (p.Arg1676=)
n.192G>T
14g.23415761C>ACA389037112MHRT,MYH7c.5025G>T (p.Glu1675Asp)
n.193C>A
14g.23415761C>GCA389037113MHRT,MYH7c.5025G>C (p.Glu1675Asp)
n.193C>G
14g.23415761C>TCA485766219MHRT,MYH7c.5025G>A (p.Glu1675=)
n.193C>T
14g.23415762T>ACA389037114MHRT,MYH7c.5024A>T (p.Glu1675Val)
n.194T>A
14g.23415762T>CCA389037115MHRT,MYH7c.5024A>G (p.Glu1675Gly)
n.194T>C
gnomAD v4
14g.23415762T>GCA389037116MHRT,MYH7c.5024A>C (p.Glu1675Ala)
n.194T>G
14g.23415763C>ACA389037117MHRT,MYH7c.5023G>T (p.Glu1675Ter)
n.195C>A
14g.23415763C>GCA389037118MHRT,MYH7c.5023G>C (p.Glu1675Gln)
n.195C>G
14g.23415763C>TCA389037119MHRT,MYH7c.5023G>A (p.Glu1675Lys)
n.195C>T
14g.23415764C>ACA485766226MHRT,MYH7c.5022G>T (p.Val1674=)
n.196C>A
14g.23415764C>GCA485766227MHRT,MYH7c.5022G>C (p.Val1674=)
n.196C>G
14g.23415764C>TCA485766228MHRT,MYH7c.5022G>A (p.Val1674=)
n.196C>T
14g.23415765A>CCA389037120MHRT,MYH7c.5021T>G (p.Val1674Gly)
n.197A>C
14g.23415765A>GCA389037121MHRT,MYH7c.5021T>C (p.Val1674Ala)
n.197A>G
14g.23415765A>TCA389037122MHRT,MYH7c.5021T>A (p.Val1674Glu)
n.197A>T
ClinVar dbSNP
14g.23415765_23415771delinsACGATGGCA2123464339MHRT,MYH7c.5015_5021delinsCCATCGT (p.Ala1672=)
n.197_203delinsACGATGG
14g.23415766C>ACA389037124MHRT,MYH7c.5020G>T (p.Val1674Leu)
n.198C>A
ClinVar dbSNP gnomAD v4
14g.23415766C=CA2123464350MHRT,MYH7c.5020G= (p.Val1674=)
n.198C=
14g.23415766C>GCA389037123MHRT,MYH7c.5020G>C (p.Val1674Leu)
n.198C>G
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23415766C>TCA015575MHRT,MYH7c.5020G>A (p.Val1674Met)
n.198C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415771_23415776delCA015559MHRT,MYH7c.5015_5020del (p.Ala1672_Ile1673del)
n.203_208del
ClinVar dbSNP
14g.23415767G>ACA044845MHRT,MYH7c.5019C>T (p.Ile1673=)
n.199G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415767G>CCA389037125MHRT,MYH7c.5019C>G (p.Ile1673Met)
n.199G>C
gnomAD v4
14g.23415767G=CA2123464368MHRT,MYH7c.5019C= (p.Ile1673=)
n.199G=
14g.23415767G>TCA485766234MHRT,MYH7c.5019C>A (p.Ile1673=)
n.199G>T
14g.23415768A>CCA389037126MHRT,MYH7c.5018T>G (p.Ile1673Ser)
n.200A>C
14g.23415768A>GCA389037127MHRT,MYH7c.5018T>C (p.Ile1673Thr)
n.200A>G
14g.23415768A>TCA389037128MHRT,MYH7c.5018T>A (p.Ile1673Asn)
n.200A>T
14g.23415769T>ACA015565MHRT,MYH7c.5017A>T (p.Ile1673Phe)
n.201T>A
ClinVar dbSNP
14g.23415769T>CCA044805MHRT,MYH7c.5017A>G (p.Ile1673Val)
n.201T>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23415769T>GCA389037129MHRT,MYH7c.5017A>C (p.Ile1673Leu)
n.201T>G
14g.23415769T=CA2123464374MHRT,MYH7c.5017A= (p.Ile1673=)
n.201T=
14g.23415770G>ACA485766239MHRT,MYH7c.5016C>T (p.Ala1672=)
n.202G>A
14g.23415770G>CCA485766242MHRT,MYH7c.5016C>G (p.Ala1672=)
n.202G>C
ClinVar gnomAD v4
14g.23415770G=CA2123464379MHRT,MYH7c.5016C= (p.Ala1672=)
n.202G=
14g.23415770G>TCA257809940MHRT,MYH7c.5016C>A (p.Ala1672=)
n.202G>T
dbSNP
14g.23415771G>ACA389037130MHRT,MYH7c.5015C>T (p.Ala1672Val)
n.203G>A
ClinVar dbSNP gnomAD v4
14g.23415771G>CCA389037131MHRT,MYH7c.5015C>G (p.Ala1672Gly)
n.203G>C
14g.23415771G>TCA389037132MHRT,MYH7c.5015C>A (p.Ala1672Asp)
n.203G>T
14g.23415772C>ACA389037133MHRT,MYH7c.5014G>T (p.Ala1672Ser)
n.204C>A
14g.23415772C=CA2123464388MHRT,MYH7c.5014G= (p.Ala1672=)
n.204C=
14g.23415772C>GCA389037134MHRT,MYH7c.5014G>C (p.Ala1672Pro)
n.204C>G
14g.23415772C>TCA044783MHRT,MYH7c.5014G>A (p.Ala1672Thr)
n.204C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415773G>ACA044766MHRT,MYH7c.5013C>T (p.Ile1671=)
n.205G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
14g.23415773G>CCA044755MHRT,MYH7c.5013C>G (p.Ile1671Met)
n.205G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415773G=CA2123464400MHRT,MYH7c.5013C= (p.Ile1671=)
n.205G=
14g.23415773G>TCA485766247MHRT,MYH7c.5013C>A (p.Ile1671=)
n.205G>T
14g.23415774A=CA2123464404MHRT,MYH7c.5012T= (p.Ile1671=)
n.206A=
14g.23415774A>CCA389037135MHRT,MYH7c.5012T>G (p.Ile1671Ser)
n.206A>C
14g.23415774A>GCA015551MHRT,MYH7c.5012T>C (p.Ile1671Thr)
n.206A>G
dbSNP
14g.23415774A>TCA389037136MHRT,MYH7c.5012T>A (p.Ile1671Asn)
n.206A>T
14g.23415775T>ACA389037137MHRT,MYH7c.5011A>T (p.Ile1671Phe)
n.207T>A
14g.23415775T>CCA389037138MHRT,MYH7c.5011A>G (p.Ile1671Val)
n.207T>C
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23415775T>GCA389037139MHRT,MYH7c.5011A>C (p.Ile1671Leu)
n.207T>G
ClinVar dbSNP
14g.23415775T=CA2123464413MHRT,MYH7c.5011A= (p.Ile1671=)
n.207T=
14g.23415776G>ACA044742MHRT,MYH7c.5010C>T (p.Asn1670=)
n.208G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415776G>CCA389037140MHRT,MYH7c.5010C>G (p.Asn1670Lys)
n.208G>C
14g.23415776G=CA2123464425MHRT,MYH7c.5010C= (p.Asn1670=)
n.208G=
14g.23415776G>TCA389037141MHRT,MYH7c.5010C>A (p.Asn1670Lys)
n.208G>T
14g.23415777T>ACA389037142MHRT,MYH7c.5009A>T (p.Asn1670Ile)
n.209T>A
14g.23415777T>CCA389037143MHRT,MYH7c.5009A>G (p.Asn1670Ser)
n.209T>C
14g.23415777T>GCA389037144MHRT,MYH7c.5009A>C (p.Asn1670Thr)
n.209T>G
14g.23415778T>ACA389037146MHRT,MYH7c.5008A>T (p.Asn1670Tyr)
n.210T>A
14g.23415778T>CCA389037147MHRT,MYH7c.5008A>G (p.Asn1670Asp)
n.210T>C
14g.23415778T>GCA389037145MHRT,MYH7c.5008A>C (p.Asn1670His)
n.210T>G
14g.23415778_23415781delinsTCTCCA2123464428MHRT,MYH7c.5005_5008delinsGAGA (p.Glu1669=)
n.210_213delinsTCTC
14g.23415779C>ACA389037148MHRT,MYH7c.5007G>T (p.Glu1669Asp)
n.211C>A
14g.23415779C>GCA389037149MHRT,MYH7c.5007G>C (p.Glu1669Asp)
n.211C>G
14g.23415779C>TCA485766259MHRT,MYH7c.5007G>A (p.Glu1669=)
n.211C>T
14g.23415781_23415783delCA015545MHRT,MYH7c.5005_5007del (p.Glu1669del)
n.213_215del
ClinVar dbSNP
14g.23415780T>ACA389037150MHRT,MYH7c.5006A>T (p.Glu1669Val)
n.212T>A
14g.23415780T>CCA389037151MHRT,MYH7c.5006A>G (p.Glu1669Gly)
n.212T>C
gnomAD v4
14g.23415780T>GCA389037152MHRT,MYH7c.5006A>C (p.Glu1669Ala)
n.212T>G
14g.23415781C>ACA257809989MHRT,MYH7c.5005G>T (p.Glu1669Ter)
n.213C>A
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23415781C=CA2123464439MHRT,MYH7c.5005G= (p.Glu1669=)
n.213C=
14g.23415781C>GCA389037153MHRT,MYH7c.5005G>C (p.Glu1669Gln)
n.213C>G
14g.23415781C>TCA389037154MHRT,MYH7c.5005G>A (p.Glu1669Lys)
n.213C>T
COSMIC
14g.23415782C>ACA389037155MHRT,MYH7c.5004G>T (p.Lys1668Asn)
n.214C>A
ClinVar
14g.23415782C=CA2123464444MHRT,MYH7c.5004G= (p.Lys1668=)
n.214C=
14g.23415782C>GCA389037156MHRT,MYH7c.5004G>C (p.Lys1668Asn)
n.214C>G
14g.23415782C>TCA044704MHRT,MYH7c.5004G>A (p.Lys1668=)
n.214C>T
ClinVar dbSNP ExAC gnomAD v4 COSMIC
14g.23415783T>ACA389037157MHRT,MYH7c.5003A>T (p.Lys1668Met)
n.215T>A
14g.23415783T>CCA389037158MHRT,MYH7c.5003A>G (p.Lys1668Arg)
n.215T>C
dbSNP gnomAD v2 gnomAD v4
14g.23415783T>GCA389037159MHRT,MYH7c.5003A>C (p.Lys1668Thr)
n.215T>G
14g.23415783T=CA2123464449MHRT,MYH7c.5003A= (p.Lys1668=)
n.215T=
14g.23415784T>ACA389037162MHRT,MYH7c.5002A>T (p.Lys1668Ter)
n.216T>A
14g.23415784T>CCA389037160MHRT,MYH7c.5002A>G (p.Lys1668Glu)
n.216T>C
ClinVar dbSNP
14g.23415784T>GCA389037161MHRT,MYH7c.5002A>C (p.Lys1668Gln)
n.216T>G
14g.23415784T=CA2123464454MHRT,MYH7c.5002A= (p.Lys1668=)
n.216T=
14g.23415785C>ACA485766271MHRT,MYH7c.5001G>T (p.Leu1667=)
n.217C>A
14g.23415785C=CA2123464459MHRT,MYH7c.5001G= (p.Leu1667=)
n.217C=
14g.23415785C>GCA485766273MHRT,MYH7c.5001G>C (p.Leu1667=)
n.217C>G
14g.23415785C>TCA485766274MHRT,MYH7c.5001G>A (p.Leu1667=)
n.217C>T
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23415786A>CCA389037163MHRT,MYH7c.5000T>G (p.Leu1667Arg)
n.218A>C
14g.23415786A>GCA389037164MHRT,MYH7c.5000T>C (p.Leu1667Pro)
n.218A>G
14g.23415786A>TCA389037165MHRT,MYH7c.5000T>A (p.Leu1667Gln)
n.218A>T
14g.23415787G>ACA485766275MHRT,MYH7c.4999C>T (p.Leu1667=)
n.219G>A
14g.23415787G>CCA389037166MHRT,MYH7c.4999C>G (p.Leu1667Val)
n.219G>C
14g.23415787G>TCA389037167MHRT,MYH7c.4999C>A (p.Leu1667Met)
n.219G>T
14g.23415788G>ACA485766278MHRT,MYH7c.4998C>T (p.Asp1666=)
n.220G>A
14g.23415788G>CCA389037168MHRT,MYH7c.4998C>G (p.Asp1666Glu)
n.220G>C
14g.23415788G=CA2123464466MHRT,MYH7c.4998C= (p.Asp1666=)
n.220G=
14g.23415788G>TCA389037169MHRT,MYH7c.4998C>A (p.Asp1666Glu)
n.220G>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23415789T>ACA389037170MHRT,MYH7c.4997A>T (p.Asp1666Val)
n.221T>A
14g.23415789T>CCA389037171MHRT,MYH7c.4997A>G (p.Asp1666Gly)
n.221T>C
14g.23415789T>GCA389037172MHRT,MYH7c.4997A>C (p.Asp1666Ala)
n.221T>G
14g.23415790C>ACA389037174MHRT,MYH7c.4996G>T (p.Asp1666Tyr)
n.222C>A
14g.23415790C=CA2123464476MHRT,MYH7c.4996G= (p.Asp1666=)
n.222C=
14g.23415790C>GCA389037173MHRT,MYH7c.4996G>C (p.Asp1666His)
n.222C>G
14g.23415790C>TCA044679MHRT,MYH7c.4996G>A (p.Asp1666Asn)
n.222C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23415791G>ACA485766283MHRT,MYH7c.4995C>T (p.Asp1665=)
n.223G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23415791G>CCA389037175MHRT,MYH7c.4995C>G (p.Asp1665Glu)
n.223G>C
14g.23415791G=CA2123464487MHRT,MYH7c.4995C= (p.Asp1665=)
n.223G=
14g.23415791G>TCA389037176MHRT,MYH7c.4995C>A (p.Asp1665Glu)
n.223G>T
14g.23415792T>ACA389037177MHRT,MYH7c.4994A>T (p.Asp1665Val)
n.224T>A
14g.23415792T>CCA389037178MHRT,MYH7c.4994A>G (p.Asp1665Gly)
n.224T>C
14g.23415792T>GCA389037179MHRT,MYH7c.4994A>C (p.Asp1665Ala)
n.224T>G
14g.23415793C>ACA389037180MHRT,MYH7c.4993G>T (p.Asp1665Tyr)
n.225C>A
14g.23415793C=CA2123464494MHRT,MYH7c.4993G= (p.Asp1665=)
n.225C=
14g.23415793C>GCA389037181MHRT,MYH7c.4993G>C (p.Asp1665His)
n.225C>G
14g.23415793C>TCA044655MHRT,MYH7c.4993G>A (p.Asp1665Asn)
n.225C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
14g.23415794G>ACA044648MHRT,MYH7c.4992C>T (p.Asn1664=)
n.226G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23415794G>CCA389037182MHRT,MYH7c.4992C>G (p.Asn1664Lys)
n.226G>C
14g.23415794G=CA2123464500MHRT,MYH7c.4992C= (p.Asn1664=)
n.226G=
14g.23415794G>TCA044638MHRT,MYH7c.4992C>A (p.Asn1664Lys)
n.226G>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23415795T>ACA389037185MHRT,MYH7c.4991A>T (p.Asn1664Ile)
n.227T>A
14g.23415795T>CCA389037184MHRT,MYH7c.4991A>G (p.Asn1664Ser)
n.227T>C
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23415795T>GCA389037183MHRT,MYH7c.4991A>C (p.Asn1664Thr)
n.227T>G
14g.23415795T=CA2123464511MHRT,MYH7c.4991A= (p.Asn1664=)
n.227T=
14g.23415796T>ACA389037186MHRT,MYH7c.4990A>T (p.Asn1664Tyr)
n.228T>A
14g.23415796T>CCA389037187MHRT,MYH7c.4990A>G (p.Asn1664Asp)
n.228T>C
14g.23415796T>GCA389037188MHRT,MYH7c.4990A>C (p.Asn1664His)
n.228T>G
14g.23415797G>ACA485766293MHRT,MYH7c.4989C>T (p.Ala1663=)
n.229G>A
14g.23415797G>CCA485766294MHRT,MYH7c.4989C>G (p.Ala1663=)
n.229G>C
14g.23415797G>TCA485766295MHRT,MYH7c.4989C>A (p.Ala1663=)
n.229G>T
14g.23415798G>ACA389037189MHRT,MYH7c.4988C>T (p.Ala1663Val)
n.230G>A
ClinVar dbSNP
14g.23415798G>CCA389037190MHRT,MYH7c.4988C>G (p.Ala1663Gly)
n.230G>C
14g.23415798G=CA2123464517MHRT,MYH7c.4988C= (p.Ala1663=)
n.230G=
14g.23415798G>TCA389037191MHRT,MYH7c.4988C>A (p.Ala1663Asp)
n.230G>T
ClinVar dbSNP
14g.23415799C>ACA389037192MHRT,MYH7c.4987G>T (p.Ala1663Ser)
n.231C>A
14g.23415799C=CA2123464526MHRT,MYH7c.4987G= (p.Ala1663=)
n.231C=
14g.23415799C>GCA347268MHRT,MYH7c.4987G>C (p.Ala1663Pro)
n.231C>G
dbSNP
14g.23415799C>TCA389037193MHRT,MYH7c.4987G>A (p.Ala1663Thr)
n.231C>T
ClinVar
14g.23415800A>CCA485766296MHRT,MYH7c.4986T>G (p.Arg1662=)
n.232A>C
14g.23415800A>GCA485766298MHRT,MYH7c.4986T>C (p.Arg1662=)
n.232A>G
14g.23415800A>TCA485766300MHRT,MYH7c.4986T>A (p.Arg1662=)
n.232A>T
14g.23415801C>ACA16614388MHRT,MYH7c.4985G>T (p.Arg1662Leu)
n.233C>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23415801C=CA2123464538MHRT,MYH7c.4985G= (p.Arg1662=)
n.233C=
14g.23415801C>GCA015530MHRT,MYH7c.4985G>C (p.Arg1662Pro)
n.233C>G
ClinVar dbSNP
14g.23415801C>TCA015524MHRT,MYH7c.4985G>A (p.Arg1662His)
n.233C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415802G>ACA044615MHRT,MYH7c.4984C>T (p.Arg1662Cys)
n.234G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23415802G>CCA389037195MHRT,MYH7c.4984C>G (p.Arg1662Gly)
n.234G>C
14g.23415802G=CA2123464553MHRT,MYH7c.4984C= (p.Arg1662=)
n.234G=
14g.23415802G>TCA389037194MHRT,MYH7c.4984C>A (p.Arg1662Ser)
n.234G>T
14g.23415803G>ACA485766305MHRT,MYH7c.4983C>T (p.Val1661=)
n.235G>A
14g.23415803G>CCA485766306MHRT,MYH7c.4983C>G (p.Val1661=)
n.235G>C
14g.23415803G>TCA485766303MHRT,MYH7c.4983C>A (p.Val1661=)
n.235G>T
14g.23415804A>CCA389037196MHRT,MYH7c.4982T>G (p.Val1661Gly)
n.236A>C
14g.23415804A>GCA389037198MHRT,MYH7c.4982T>C (p.Val1661Ala)
n.236A>G
14g.23415804A>TCA389037197MHRT,MYH7c.4982T>A (p.Val1661Asp)
n.236A>T
14g.23415805delCA2624233546MHRT,MYH7c.4981del (p.Val1661SerfsTer7)
n.237del
gnomAD v4
14g.23415805C>ACA389037199MHRT,MYH7c.4981G>T (p.Val1661Phe)
n.237C>A
14g.23415805C=CA2123464564MHRT,MYH7c.4981G= (p.Val1661=)
n.237C=
14g.23415805C>GCA389037200MHRT,MYH7c.4981G>C (p.Val1661Leu)
n.237C>G
ClinVar dbSNP
14g.23415805C>TCA389037201MHRT,MYH7c.4981G>A (p.Val1661Ile)
n.237C>T
ClinVar dbSNP gnomAD v4
14g.23415806T>ACA485766311MHRT,MYH7c.4980A>T (p.Ala1660=)
n.238T>A
14g.23415806T>CCA044604MHRT,MYH7c.4980A>G (p.Ala1660=)
n.238T>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415806T>GCA015515MHRT,MYH7c.4980A>C (p.Ala1660=)
n.238T>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415806T=CA2123464574MHRT,MYH7c.4980A= (p.Ala1660=)
n.238T=
14g.23415807G>ACA389037203MHRT,MYH7c.4979C>T (p.Ala1660Val)
n.239G>A
dbSNP
14g.23415807G>CCA389037202MHRT,MYH7c.4979C>G (p.Ala1660Gly)
n.239G>C
14g.23415807G=CA2123464582MHRT,MYH7c.4979C= (p.Ala1660=)
n.239G=
14g.23415807G>TCA257810052MHRT,MYH7c.4979C>A (p.Ala1660Glu)
n.239G>T
ClinVar dbSNP gnomAD v4
14g.23415808C>ACA389037204MHRT,MYH7c.4978G>T (p.Ala1660Ser)
n.240C>A
14g.23415808C=CA2123464584MHRT,MYH7c.4978G= (p.Ala1660=)
n.240C=
14g.23415808C>GCA389037205MHRT,MYH7c.4978G>C (p.Ala1660Pro)
n.240C>G
ClinVar dbSNP
14g.23415808C>TCA389037206MHRT,MYH7c.4978G>A (p.Ala1660Thr)
n.240C>T
gnomAD v4
14g.23415809A=CA2123464589MHRT,MYH7c.4977T= (p.Asp1659=)
n.241A=
14g.23415809A>CCA389037207MHRT,MYH7c.4977T>G (p.Asp1659Glu)
n.241A>C
14g.23415809A>GCA044584MHRT,MYH7c.4977T>C (p.Asp1659=)
n.241A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23415809A>TCA389037208MHRT,MYH7c.4977T>A (p.Asp1659Glu)
n.241A>T
dbSNP gnomAD v4
14g.23415810T>ACA389037211MHRT,MYH7c.4976A>T (p.Asp1659Val)
n.242T>A
14g.23415810T>CCA389037209MHRT,MYH7c.4976A>G (p.Asp1659Gly)
n.242T>C
14g.23415810T>GCA389037210MHRT,MYH7c.4976A>C (p.Asp1659Ala)
n.242T>G
14g.23415811C>ACA389037212MHRT,MYH7c.4975G>T (p.Asp1659Tyr)
n.243C>A
dbSNP
14g.23415811C=CA2123464595MHRT,MYH7c.4975G= (p.Asp1659=)
n.243C=
14g.23415811C>GCA389037213MHRT,MYH7c.4975G>C (p.Asp1659His)
n.243C>G
14g.23415811C>TCA044566MHRT,MYH7c.4975G>A (p.Asp1659Asn)
n.243C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23415811_23415812delinsCGCA2123464599MHRT,MYH7c.4974_4975delinsCG (p.Asp1658=)
n.243_244delinsCG
14g.23415812delCA2123464604MHRT,MYH7c.4974del (p.Asp1658GlufsTer10)
n.244del
dbSNP
14g.23415812G>ACA015510MHRT,MYH7c.4974C>T (p.Asp1658=)
n.244G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23415812G>CCA389037214MHRT,MYH7c.4974C>G (p.Asp1658Glu)
n.244G>C
14g.23415812G=CA2123464606MHRT,MYH7c.4974C= (p.Asp1658=)
n.244G=
14g.23415812G>TCA389037215MHRT,MYH7c.4974C>A (p.Asp1658Glu)
n.244G>T
14g.23415813T>ACA389037216MHRT,MYH7c.4973A>T (p.Asp1658Val)
n.245T>A
14g.23415813T>CCA389037217MHRT,MYH7c.4973A>G (p.Asp1658Gly)
n.245T>C
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23415813T>GCA389037218MHRT,MYH7c.4973A>C (p.Asp1658Ala)
n.245T>G
14g.23415813T=CA2123464617MHRT,MYH7c.4973A= (p.Asp1658=)
n.245T=
14g.23415814C>ACA389037219MHRT,MYH7c.4972G>T (p.Asp1658Tyr)
n.246C>A
14g.23415814C>GCA389037220MHRT,MYH7c.4972G>C (p.Asp1658His)
n.246C>G
14g.23415814C>TCA389037221MHRT,MYH7c.4972G>A (p.Asp1658Asn)
n.246C>T
ClinVar
14g.23415815C>ACA485766333MHRT,MYH7c.4971G>T (p.Leu1657=)
n.247C>A
14g.23415815C>GCA485766329MHRT,MYH7c.4971G>C (p.Leu1657=)
n.247C>G
14g.23415815C>TCA485766335MHRT,MYH7c.4971G>A (p.Leu1657=)
n.247C>T
14g.23415816A>CCA389037222MHRT,MYH7c.4970T>G (p.Leu1657Arg)
n.248A>C
14g.23415816A>GCA389037224MHRT,MYH7c.4970T>C (p.Leu1657Pro)
n.248A>G
ClinVar dbSNP
14g.23415816A>TCA389037223MHRT,MYH7c.4970T>A (p.Leu1657Gln)
n.248A>T
14g.23415817G>ACA485766338MHRT,MYH7c.4969C>T (p.Leu1657=)
n.249G>A
14g.23415817G>CCA389037225MHRT,MYH7c.4969C>G (p.Leu1657Val)
n.249G>C
14g.23415817G>TCA389037226MHRT,MYH7c.4969C>A (p.Leu1657Met)
n.249G>T
14g.23415818C>ACA389037227MHRT,MYH7c.4968G>T (p.Gln1656His)
n.250C>A
14g.23415818C>GCA389037228MHRT,MYH7c.4968G>C (p.Gln1656His)
n.250C>G
14g.23415818C>TCA485766341MHRT,MYH7c.4968G>A (p.Gln1656=)
n.250C>T
14g.23415819T>ACA389037229MHRT,MYH7c.4967A>T (p.Gln1656Leu)
n.251T>A
14g.23415819T>CCA389037230MHRT,MYH7c.4967A>G (p.Gln1656Arg)
n.251T>C
14g.23415819T>GCA389037231MHRT,MYH7c.4967A>C (p.Gln1656Pro)
n.251T>G
14g.23415820G>ACA389037232MHRT,MYH7c.4966C>T (p.Gln1656Ter)
n.252G>A
ClinVar dbSNP gnomAD v4
14g.23415820G>CCA389037233MHRT,MYH7c.4966C>G (p.Gln1656Glu)
n.252G>C
ClinVar dbSNP
14g.23415820G=CA2123464632MHRT,MYH7c.4966C= (p.Gln1656=)
n.252G=
14g.23415820G>TCA389037234MHRT,MYH7c.4966C>A (p.Gln1656Lys)
n.252G>T
14g.23415821A=CA2123464636MHRT,MYH7c.4965T= (p.Ile1655=)
n.253A=
14g.23415821A>CCA389037235MHRT,MYH7c.4965T>G (p.Ile1655Met)
n.253A>C
14g.23415821A>GCA10587765MHRT,MYH7c.4965T>C (p.Ile1655=)
n.253A>G
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23415821A>TCA485766346MHRT,MYH7c.4965T>A (p.Ile1655=)
n.253A>T
14g.23415822A=CA2123464639MHRT,MYH7c.4964T= (p.Ile1655=)
n.254A=
14g.23415822A>CCA389037238MHRT,MYH7c.4964T>G (p.Ile1655Ser)
n.254A>C
14g.23415822A>GCA389037236MHRT,MYH7c.4964T>C (p.Ile1655Thr)
n.254A>G
ClinVar dbSNP
14g.23415822A>TCA389037237MHRT,MYH7c.4964T>A (p.Ile1655Asn)
n.254A>T
14g.23415823T>ACA389037239MHRT,MYH7c.4963A>T (p.Ile1655Phe)
n.255T>A
14g.23415823T>CCA389037240MHRT,MYH7c.4963A>G (p.Ile1655Val)
n.255T>C
14g.23415823T>GCA389037241MHRT,MYH7c.4963A>C (p.Ile1655Leu)
n.255T>G
14g.23415824C>ACA389037242MHRT,MYH7c.4962G>T (p.Gln1654His)
n.256C>A
14g.23415824C>GCA389037243MHRT,MYH7c.4962G>C (p.Gln1654His)
n.256C>G
14g.23415824C>TCA485766351MHRT,MYH7c.4962G>A (p.Gln1654=)
n.256C>T
14g.23415825T>ACA389037244MHRT,MYH7c.4961A>T (p.Gln1654Leu)
n.257T>A
14g.23415825T>CCA389037245MHRT,MYH7c.4961A>G (p.Gln1654Arg)
n.257T>C
COSMIC
14g.23415825T>GCA389037246MHRT,MYH7c.4961A>C (p.Gln1654Pro)
n.257T>G
14g.23415826G>ACA389037247MHRT,MYH7c.4960C>T (p.Gln1654Ter)
n.258G>A
ClinVar dbSNP
14g.23415826G>CCA389037248MHRT,MYH7c.4960C>G (p.Gln1654Glu)
n.258G>C
14g.23415826G=CA2123464648MHRT,MYH7c.4960C= (p.Gln1654=)
n.258G=
14g.23415826G>TCA389037249MHRT,MYH7c.4960C>A (p.Gln1654Lys)
n.258G>T
14g.23415828delCA2580087965MHRT,MYH7c.4960del (p.Gln1654ArgfsTer14)
n.260del
ClinVar
14g.23415827G>ACA485766357MHRT,MYH7c.4959C>T (p.Thr1653=)
n.259G>A
14g.23415827G>CCA485766358MHRT,MYH7c.4959C>G (p.Thr1653=)
n.259G>C
14g.23415827G>TCA485766359MHRT,MYH7c.4959C>A (p.Thr1653=)
n.259G>T
14g.23415828G>ACA389037252MHRT,MYH7c.4958C>T (p.Thr1653Ile)
n.260G>A
14g.23415828G>CCA389037251MHRT,MYH7c.4958C>G (p.Thr1653Ser)
n.260G>C
14g.23415828G>TCA389037250MHRT,MYH7c.4958C>A (p.Thr1653Asn)
n.260G>T
14g.23415831_23415850delCA2573053877MHRT,MYH7c.4954-15_4958del
n.261+2_261+21del
ClinVar dbSNP
14g.23415829T>ACA389037253MHRT,MYH7c.4957A>T (p.Thr1653Ser)
n.261T>A
14g.23415829T>CCA389037255MHRT,MYH7c.4957A>G (p.Thr1653Ala)
n.261T>C
14g.23415829T>GCA389037254MHRT,MYH7c.4957A>C (p.Thr1653Pro)
n.261T>G
14g.23415830G>ACA485766361MHRT,MYH7c.4956C>T (p.Asp1652=)
n.261+1G>A
14g.23415830G>CCA389037256MHRT,MYH7c.4956C>G (p.Asp1652Glu)
n.261+1G>C
14g.23415830G>TCA389037257MHRT,MYH7c.4956C>A (p.Asp1652Glu)
n.261+1G>T
14g.23415831T>ACA389037258MHRT,MYH7c.4955A>T (p.Asp1652Val)
n.261+2T>A
14g.23415831T>CCA389037259MHRT,MYH7c.4955A>G (p.Asp1652Gly)
n.261+2T>C
14g.23415831T>GCA389037260MHRT,MYH7c.4955A>C (p.Asp1652Ala)
n.261+2T>G
ClinVar dbSNP
14g.23415832C>ACA015501MHRT,MYH7c.4954G>T (p.Asp1652Tyr)
n.261+3C>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415832C=CA2123464658MHRT,MYH7c.4954G= (p.Asp1652=)
n.261+3C=
14g.23415832C>GCA389037261MHRT,MYH7c.4954G>C (p.Asp1652His)
n.261+3C>G
14g.23415832C>TCA044527MHRT,MYH7c.4954G>A (p.Asp1652Asn)
n.261+3C>T
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23415833C>ACA389037262MHRT,MYH7c.4954-1G>T (n.4954-1G>T)
n.261+4C>A
14g.23415833C>GCA389037263MHRT,MYH7c.4954-1G>C (n.4954-1G>C)
n.261+4C>G
14g.23415833C>TCA389037264MHRT,MYH7c.4954-1G>A (n.4954-1G>A)
n.261+4C>T
14g.23415834T>ACA389037267MHRT,MYH7c.4954-2A>T (n.4954-2A>T)
n.261+5T>A
14g.23415834T>CCA389037266MHRT,MYH7c.4954-2A>G (n.4954-2A>G)
n.261+5T>C
14g.23415834T>GCA389037265MHRT,MYH7c.4954-2A>C (n.4954-2A>C)
n.261+5T>G
14g.23415835G>CCA257810104MHRT,MYH7c.4954-3C>G (n.4954-3C>G)
n.261+6G>C
dbSNP
14g.23415835G=CA2123464674MHRT,MYH7c.4954-3C= (n.4954-3C=)
n.261+6G=
14g.23415835G>TCA257810105MHRT,MYH7c.4954-3C>A (n.4954-3C>A)
n.261+6G>T
dbSNP
14g.23415836A>GCA2580087966MHRT,MYH7c.4954-4T>C (n.4954-4T>C)
n.261+7A>G
ClinVar
14g.23415837G>ACA257810106MHRT,MYH7c.4954-5C>T (n.4954-5C>T)
n.261+8G>A
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23415837G>CCA2123464686MHRT,MYH7c.4954-5C>G (n.4954-5C>G)
n.261+8G>C
ClinVar dbSNP gnomAD v4
14g.23415837G=CA2123464684MHRT,MYH7c.4954-5C= (n.4954-5C=)
n.261+8G=
14g.23415838delCA2580087967MHRT,MYH7c.4954-5del (n.4954-5del)
n.261+9del
ClinVar gnomAD v4
14g.23415838G>ACA2624233649MHRT,MYH7c.4954-6C>T (n.4954-6C>T)
n.261+9G>A
gnomAD v4
14g.23415838G>CCA2123464694MHRT,MYH7c.4954-6C>G (n.4954-6C>G)
n.261+9G>C
ClinVar dbSNP gnomAD v4
14g.23415838G=CA2123464693MHRT,MYH7c.4954-6C= (n.4954-6C=)
n.261+9G=
14g.23415839A=CA2123464695MHRT,MYH7c.4954-7T= (n.4954-7T=)
n.261+10A=
14g.23415839A>TCA2123464696MHRT,MYH7c.4954-7T>A (n.4954-7T>A)
n.261+10A>T
dbSNP gnomAD v4
14g.23415840T>GCA2580087968MHRT,MYH7c.4954-8A>C (n.4954-8A>C)
n.261+11T>G
ClinVar
14g.23415841C=CA2123464699MHRT,MYH7c.4954-9G= (n.4954-9G=)
n.261+12C=
14g.23415841C>GCA2123464714MHRT,MYH7c.4954-9G>C (n.4954-9G>C)
n.261+12C>G
ClinVar dbSNP gnomAD v4
14g.23415841C>TCA2575486432MHRT,MYH7c.4954-9G>A (n.4954-9G>A)
n.261+12C>T
gnomAD v4
14g.23415842A=CA2123464717MHRT,MYH7c.4954-10T= (n.4954-10T=)
n.261+13A=
14g.23415842A>GCA2123464718MHRT,MYH7c.4954-10T>C (n.4954-10T>C)
n.261+13A>G
dbSNP gnomAD v4
14g.23415843G>TCA2624233660MHRT,MYH7c.4954-11C>A (n.4954-11C>A)
n.261+14G>T
gnomAD v4
14g.23415844G>ACA613317700MHRT,MYH7c.4954-12C>T (n.4954-12C>T)
n.261+15G>A
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23415844G=CA2123464720MHRT,MYH7c.4954-12C= (n.4954-12C=)
n.261+15G=
14g.23415846G>ACA658798172MHRT,MYH7c.4954-14C>T (n.4954-14C>T)
n.261+17G>A
ClinVar dbSNP gnomAD v4
14g.23415846G>CCA015494MHRT,MYH7c.4954-14C>G (n.4954-14C>G)
n.261+17G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23415846G=CA2123464733MHRT,MYH7c.4954-14C= (n.4954-14C=)
n.261+17G=
14g.23415847A=CA2123464737MHRT,MYH7c.4954-15T= (n.4954-15T=)
n.261+18A=
14g.23415847A>GCA961068499MHRT,MYH7c.4954-15T>C (n.4954-15T>C)
n.261+18A>G
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23415848G>ACA2624233679MHRT,MYH7c.4954-16C>T (n.4954-16C>T)
n.261+19G>A
gnomAD v4
14g.23415848G>CCA2123464741MHRT,MYH7c.4954-16C>G (n.4954-16C>G)
n.261+19G>C
ClinVar dbSNP gnomAD v4
14g.23415848G=CA2123464740MHRT,MYH7c.4954-16C= (n.4954-16C=)
n.261+19G=
14g.23415849T>CCA656016645MHRT,MYH7c.4954-17A>G (n.4954-17A>G)
n.261+20T>C
gnomAD v4 COSMIC COSMIC
14g.23415850G>CCA613317701MHRT,MYH7c.4954-18C>G (n.4954-18C>G)
n.261+21G>C
dbSNP gnomAD v2 gnomAD v4
14g.23415850G=CA2123464742MHRT,MYH7c.4954-18C= (n.4954-18C=)
n.261+21G=
14g.23415851G>ACA2624233692MHRT,MYH7c.4954-19C>T (n.4954-19C>T)
n.261+22G>A
gnomAD v4
14g.23415851G>CCA044422MHRT,MYH7c.4954-19C>G (n.4954-19C>G)
n.261+22G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415851G=CA2123464744MHRT,MYH7c.4954-19C= (n.4954-19C=)
n.261+22G=
14g.23415851G>TCA2573149770MHRT,MYH7c.4954-19C>A (n.4954-19C>A)
n.261+22G>T
ClinVar dbSNP
14g.23415852G=CA2123464745MHRT,MYH7c.4954-20C= (n.4954-20C=)
n.261+23G=
14g.23415852G>TCA613317702MHRT,MYH7c.4954-20C>A (n.4954-20C>A)
n.261+23G>T
dbSNP gnomAD v2 gnomAD v4
14g.23415853C=CA2123464746MHRT,MYH7c.4954-21G= (n.4954-21G=)
n.261+24C=
14g.23415853C>TCA2123464748MHRT,MYH7c.4954-21G>A (n.4954-21G>A)
n.261+24C>T
dbSNP gnomAD v4
14g.23415854A=CA2123464754MHRT,MYH7c.4954-22T= (n.4954-22T=)
n.261+25A=
14g.23415854A>GCA613317703MHRT,MYH7c.4954-22T>C (n.4954-22T>C)
n.261+25A>G
dbSNP gnomAD v2 gnomAD v4
14g.23415855T>ACA656016648MHRT,MYH7c.4954-23A>T (n.4954-23A>T)
n.261+26T>A
COSMIC
14g.23415856G>ACA2123464759MHRT,MYH7c.4954-24C>T (n.4954-24C>T)
n.261+27G>A
dbSNP
14g.23415856G=CA2123464757MHRT,MYH7c.4954-24C= (n.4954-24C=)
n.261+27G=
14g.23415856G>TCA044439MHRT,MYH7c.4954-24C>A (n.4954-24C>A)
n.261+27G>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415860_23415866delCA2624233704MHRT,MYH7c.4954-30_4954-24del (n.4954-30_4954-24del)
n.261+31_261+37del
gnomAD v4

Number of alleles fetched