Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23413799A>CCA389034552MYH7c.5750T>G (p.Val1917Gly)
14g.23413799A>GCA389034553MYH7c.5750T>C (p.Val1917Ala)
14g.23413799A>TCA389034554MYH7c.5750T>A (p.Val1917Asp)
14g.23413800C>ACA016449MYH7c.5749G>T (p.Val1917Phe)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23413800C=CA2123458161MYH7c.5749G= (p.Val1917=)
14g.23413800C>GCA389034555MYH7c.5749G>C (p.Val1917Leu)
14g.23413800C>TCA389034556MYH7c.5749G>A (p.Val1917Ile)
14g.23413801C>ACA389034557MYH7c.5748G>T (p.Gln1916His)
14g.23413801C>GCA389034558MYH7c.5748G>C (p.Gln1916His)
ClinVar
14g.23413801C>TCA485616105MYH7c.5748G>A (p.Gln1916=)
14g.23413803_23413808delCA2573053875MYH7c.5743_5748del (p.Ser1915_Gln1916del)
ClinVar dbSNP
14g.23413802T>ACA389034559MYH7c.5747A>T (p.Gln1916Leu)
14g.23413802T>CCA389034560MYH7c.5747A>G (p.Gln1916Arg)
14g.23413802T>GCA389034561MYH7c.5747A>C (p.Gln1916Pro)
14g.23413803G>ACA389034562MYH7c.5746C>T (p.Gln1916Ter)
ClinVar dbSNP
14g.23413803G>CCA389034563MYH7c.5746C>G (p.Gln1916Glu)
14g.23413803G=CA2123458178MYH7c.5746C= (p.Gln1916=)
14g.23413803G>TCA389034564MYH7c.5746C>A (p.Gln1916Lys)
14g.23413804G>ACA485616110MYH7c.5745C>T (p.Ser1915=)
ClinVar dbSNP
14g.23413804G>CCA485616111MYH7c.5745C>G (p.Ser1915=)
14g.23413804G>TCA485616109MYH7c.5745C>A (p.Ser1915=)
14g.23413804_23413808delinsGGACTCA2123458186MYH7c.5741_5745delinsAGTCC (p.Glu1914=)
14g.23413805G>ACA389034565MYH7c.5744C>T (p.Ser1915Phe)
14g.23413805G>CCA389034566MYH7c.5744C>G (p.Ser1915Cys)
ClinVar
14g.23413805G>TCA389034567MYH7c.5744C>A (p.Ser1915Tyr)
14g.23413805_23413808delinsACA351898MYH7c.5741_5744delinsT (p.Glu1914_Ser1915delinsVal)
ClinVar dbSNP
14g.23413806A>CCA389034568MYH7c.5743T>G (p.Ser1915Ala)
14g.23413806A>GCA389034569MYH7c.5743T>C (p.Ser1915Pro)
14g.23413806A>TCA389034570MYH7c.5743T>A (p.Ser1915Thr)
14g.23413807C>ACA389034571MYH7c.5742G>T (p.Glu1914Asp)
ClinVar dbSNP gnomAD v4
14g.23413807C>GCA389034572MYH7c.5742G>C (p.Glu1914Asp)
14g.23413807C>TCA485616115MYH7c.5742G>A (p.Glu1914=)
ClinVar dbSNP gnomAD v4 COSMIC
14g.23413808T>ACA389034575MYH7c.5741A>T (p.Glu1914Val)
14g.23413808T>CCA389034573MYH7c.5741A>G (p.Glu1914Gly)
14g.23413808T>GCA389034574MYH7c.5741A>C (p.Glu1914Ala)
gnomAD v4
14g.23413809C>ACA389034576MYH7c.5740G>T (p.Glu1914Ter)
ClinVar dbSNP
14g.23413809C=CA2123458197MYH7c.5740G= (p.Glu1914=)
14g.23413809C>GCA389034577MYH7c.5740G>C (p.Glu1914Gln)
14g.23413809C>TCA016441MYH7c.5740G>A (p.Glu1914Lys)
ClinVar dbSNP
14g.23413810G>ACA016434MYH7c.5739C>T (p.Ala1913=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413810G>CCA048139MYH7c.5739C>G (p.Ala1913=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413810G=CA2123458210MYH7c.5739C= (p.Ala1913=)
14g.23413810G>TCA485616117MYH7c.5739C>A (p.Ala1913=)
dbSNP
14g.23413811G>ACA389034578MYH7c.5738C>T (p.Ala1913Val)
dbSNP gnomAD v2
14g.23413811G>CCA389034580MYH7c.5738C>G (p.Ala1913Gly)
14g.23413811G=CA2123458218MYH7c.5738C= (p.Ala1913=)
14g.23413811G>TCA389034579MYH7c.5738C>A (p.Ala1913Asp)
14g.23413812C>ACA389034581MYH7c.5737G>T (p.Ala1913Ser)
14g.23413812C=CA2123458224MYH7c.5737G= (p.Ala1913=)
14g.23413812C>GCA389034582MYH7c.5737G>C (p.Ala1913Pro)
14g.23413812C>TCA048119MYH7c.5737G>A (p.Ala1913Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413813G>ACA016427MYH7c.5736C>T (p.Ile1912=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413813G>CCA389034583MYH7c.5736C>G (p.Ile1912Met)
14g.23413813G=CA2123458229MYH7c.5736C= (p.Ile1912=)
14g.23413813G>TCA485616119MYH7c.5736C>A (p.Ile1912=)
dbSNP
14g.23413814delCA2573053876MYH7c.5735del (p.Ile1912ThrfsTer21)
ClinVar dbSNP
14g.23413814A=CA2123458232MYH7c.5735T= (p.Ile1912=)
14g.23413814A>CCA389034584MYH7c.5735T>G (p.Ile1912Ser)
14g.23413814A>GCA389034585MYH7c.5735T>C (p.Ile1912Thr)
14g.23413814A>TCA389034586MYH7c.5735T>A (p.Ile1912Asn)
ClinVar dbSNP
14g.23413815T>ACA389034587MYH7c.5734A>T (p.Ile1912Phe)
ClinVar dbSNP gnomAD v4
14g.23413815T>CCA389034588MYH7c.5734A>G (p.Ile1912Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23413815T>GCA389034589MYH7c.5734A>C (p.Ile1912Leu)
14g.23413815T=CA2123458238MYH7c.5734A= (p.Ile1912=)
14g.23413816G>ACA485616121MYH7c.5733C>T (p.Asp1911=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23413816G>CCA389034590MYH7c.5733C>G (p.Asp1911Glu)
14g.23413816G=CA2123458263MYH7c.5733C= (p.Asp1911=)
14g.23413816G>TCA389034591MYH7c.5733C>A (p.Asp1911Glu)
14g.23413817T>ACA389034592MYH7c.5732A>T (p.Asp1911Val)
14g.23413817T>CCA389034594MYH7c.5732A>G (p.Asp1911Gly)
14g.23413817T>GCA389034593MYH7c.5732A>C (p.Asp1911Ala)
14g.23413818C>ACA389034595MYH7c.5731G>T (p.Asp1911Tyr)
COSMIC
14g.23413818C>GCA389034597MYH7c.5731G>C (p.Asp1911His)
14g.23413818C>TCA389034596MYH7c.5731G>A (p.Asp1911Asn)
14g.23413819delCA2800863467MYH7c.5731del (p.Asp1911ThrfsTer22)
14g.23413819C>ACA485616122MYH7c.5730G>T (p.Ala1910=)
14g.23413819C=CA2123458271MYH7c.5730G= (p.Ala1910=)
14g.23413819C>GCA485616124MYH7c.5730G>C (p.Ala1910=)
14g.23413819C>TCA048097MYH7c.5730G>A (p.Ala1910=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413820G>ACA389034598MYH7c.5729C>T (p.Ala1910Val)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
14g.23413820G>CCA389034599MYH7c.5729C>G (p.Ala1910Gly)
14g.23413820G=CA2123458286MYH7c.5729C= (p.Ala1910=)
14g.23413820G>TCA389034600MYH7c.5729C>A (p.Ala1910Glu)
14g.23413821C>ACA389034601MYH7c.5728G>T (p.Ala1910Ser)
14g.23413821C>GCA389034602MYH7c.5728G>C (p.Ala1910Pro)
14g.23413821C>TCA389034603MYH7c.5728G>A (p.Ala1910Thr)
ClinVar dbSNP
14g.23413822C>ACA485616126MYH7c.5727G>T (p.Arg1909=)
14g.23413822C=CA2123458297MYH7c.5727G= (p.Arg1909=)
14g.23413822C>GCA485616127MYH7c.5727G>C (p.Arg1909=)
14g.23413822C>TCA048076MYH7c.5727G>A (p.Arg1909=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413823C>ACA389034604MYH7c.5726G>T (p.Arg1909Leu)
COSMIC
14g.23413823C=CA2123458307MYH7c.5726G= (p.Arg1909=)
14g.23413823C>GCA016422MYH7c.5726G>C (p.Arg1909Pro)
ClinVar dbSNP
14g.23413823C>TCA016417MYH7c.5726G>A (p.Arg1909Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
14g.23413824G>ACA048061MYH7c.5725C>T (p.Arg1909Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413824G>CCA389034605MYH7c.5725C>G (p.Arg1909Gly)
ClinVar dbSNP
14g.23413824G=CA2123458325MYH7c.5725C= (p.Arg1909=)
14g.23413824G>TCA016414MYH7c.5725C>A (p.Arg1909=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413825C>ACA389034606MYH7c.5724G>T (p.Glu1908Asp)
14g.23413825C=CA2123458335MYH7c.5724G= (p.Glu1908=)
14g.23413825C>GCA389034607MYH7c.5724G>C (p.Glu1908Asp)
14g.23413825C>TCA485616128MYH7c.5724G>A (p.Glu1908=)
ClinVar dbSNP
14g.23413826T>ACA389034608MYH7c.5723A>T (p.Glu1908Val)
ClinVar dbSNP
14g.23413826T>CCA389034609MYH7c.5723A>G (p.Glu1908Gly)
14g.23413826T>GCA389034610MYH7c.5723A>C (p.Glu1908Ala)
14g.23413826T=CA2123458354MYH7c.5723A= (p.Glu1908=)
14g.23413827C>ACA389034611MYH7c.5722G>T (p.Glu1908Ter)
14g.23413827C=CA2123458362MYH7c.5722G= (p.Glu1908=)
14g.23413827C>GCA389034612MYH7c.5722G>C (p.Glu1908Gln)
14g.23413827C>TCA389034613MYH7c.5722G>A (p.Glu1908Lys)
dbSNP
14g.23413828C>ACA389034614MYH7c.5721G>T (p.Glu1907Asp)
14g.23413828C>GCA389034615MYH7c.5721G>C (p.Glu1907Asp)
14g.23413828C>TCA485616129MYH7c.5721G>A (p.Glu1907=)
14g.23413829T>ACA389034617MYH7c.5720A>T (p.Glu1907Val)
14g.23413829T>CCA389034618MYH7c.5720A>G (p.Glu1907Gly)
14g.23413829T>GCA389034616MYH7c.5720A>C (p.Glu1907Ala)
14g.23413830C>ACA389034619MYH7c.5719G>T (p.Glu1907Ter)
14g.23413830C=CA2123458374MYH7c.5719G= (p.Glu1907=)
14g.23413830C>GCA389034620MYH7c.5719G>C (p.Glu1907Gln)
dbSNP gnomAD v4
14g.23413830C>TCA389034621MYH7c.5719G>A (p.Glu1907Lys)
14g.23413831T>ACA485616132MYH7c.5718A>T (p.Ala1906=)
14g.23413831T>CCA485616131MYH7c.5718A>G (p.Ala1906=)
dbSNP gnomAD v4
14g.23413831T>GCA016408MYH7c.5718A>C (p.Ala1906=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413831T=CA2123458388MYH7c.5718A= (p.Ala1906=)
14g.23413832G>ACA389034622MYH7c.5717C>T (p.Ala1906Val)
14g.23413832G>CCA016404MYH7c.5717C>G (p.Ala1906Gly)
ClinVar dbSNP
14g.23413832G=CA2123458406MYH7c.5717C= (p.Ala1906=)
14g.23413832G>TCA389034623MYH7c.5717C>A (p.Ala1906Glu)
14g.23413833C>ACA389034624MYH7c.5716G>T (p.Ala1906Ser)
14g.23413833C>GCA389034625MYH7c.5716G>C (p.Ala1906Pro)
14g.23413833C>TCA389034626MYH7c.5716G>A (p.Ala1906Thr)
14g.23413834C>ACA389034627MYH7c.5715G>T (p.Glu1905Asp)
14g.23413834C=CA2123458412MYH7c.5715G= (p.Glu1905=)
14g.23413834C>GCA389034628MYH7c.5715G>C (p.Glu1905Asp)
14g.23413834C>TCA485616133MYH7c.5715G>A (p.Glu1905=)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
14g.23413835T>ACA389034630MYH7c.5714A>T (p.Glu1905Val)
14g.23413835T>CCA389034631MYH7c.5714A>G (p.Glu1905Gly)
14g.23413835T>GCA389034629MYH7c.5714A>C (p.Glu1905Ala)
14g.23413836C>ACA389034632MYH7c.5713G>T (p.Glu1905Ter)
14g.23413836C>GCA389034633MYH7c.5713G>C (p.Glu1905Gln)
14g.23413836C>TCA389034634MYH7c.5713G>A (p.Glu1905Lys)
14g.23413837A>CCA389034635MYH7c.5712T>G (p.Asp1904Glu)
14g.23413837A>GCA485616134MYH7c.5712T>C (p.Asp1904=)
dbSNP
14g.23413837A>TCA389034636MYH7c.5712T>A (p.Asp1904Glu)
14g.23413838T>ACA389034639MYH7c.5711A>T (p.Asp1904Val)
14g.23413838T>CCA389034637MYH7c.5711A>G (p.Asp1904Gly)
14g.23413838T>GCA389034638MYH7c.5711A>C (p.Asp1904Ala)
14g.23413839C>ACA389034640MYH7c.5710G>T (p.Asp1904Tyr)
14g.23413839C>GCA389034641MYH7c.5710G>C (p.Asp1904His)
14g.23413839C>TCA389034642MYH7c.5710G>A (p.Asp1904Asn)
14g.23413840C>ACA485616135MYH7c.5709G>T (p.Leu1903=)
14g.23413840C=CA2123458424MYH7c.5709G= (p.Leu1903=)
14g.23413840C>GCA485616136MYH7c.5709G>C (p.Leu1903=)
14g.23413840C>TCA257807464MYH7c.5709G>A (p.Leu1903=)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23413841A>CCA389034643MYH7c.5708T>G (p.Leu1903Arg)
14g.23413841A>GCA389034644MYH7c.5708T>C (p.Leu1903Pro)
14g.23413841A>TCA389034645MYH7c.5708T>A (p.Leu1903Gln)
14g.23413842G>ACA485616137MYH7c.5707C>T (p.Leu1903=)
COSMIC
14g.23413842G>CCA389034647MYH7c.5707C>G (p.Leu1903Val)
14g.23413842G>TCA389034646MYH7c.5707C>A (p.Leu1903Met)
14g.23413843C>ACA389034648MYH7c.5706G>T (p.Glu1902Asp)
14g.23413843C>GCA389034649MYH7c.5706G>C (p.Glu1902Asp)
14g.23413843C>TCA485616138MYH7c.5706G>A (p.Glu1902=)
ClinVar dbSNP
14g.23413844T>ACA389034650MYH7c.5705A>T (p.Glu1902Val)
14g.23413844T>CCA389034651MYH7c.5705A>G (p.Glu1902Gly)
14g.23413844T>GCA389034652MYH7c.5705A>C (p.Glu1902Ala)
14g.23413845C>ACA389034653MYH7c.5704G>T (p.Glu1902Ter)
14g.23413845C=CA2123458435MYH7c.5704G= (p.Glu1902=)
14g.23413845C>GCA016398MYH7c.5704G>C (p.Glu1902Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413845C>TCA016392MYH7c.5704G>A (p.Glu1902Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23413846G>ACA016386MYH7c.5703C>T (p.His1901=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23413846G>CCA257807514MYH7c.5703C>G (p.His1901Gln)
dbSNP gnomAD v4
14g.23413846G=CA2123458461MYH7c.5703C= (p.His1901=)
14g.23413846G>TCA389034654MYH7c.5703C>A (p.His1901Gln)
14g.23413847T>ACA016379MYH7c.5702A>T (p.His1901Leu)
ClinVar dbSNP
14g.23413847T>CCA389034655MYH7c.5702A>G (p.His1901Arg)
14g.23413847T>GCA389034656MYH7c.5702A>C (p.His1901Pro)
14g.23413847T=CA2123458469MYH7c.5702A= (p.His1901=)
14g.23413848G>ACA389034658MYH7c.5701C>T (p.His1901Tyr)
14g.23413848G>CCA389034659MYH7c.5701C>G (p.His1901Asp)
14g.23413848G>TCA389034657MYH7c.5701C>A (p.His1901Asn)
14g.23413849C>ACA389034660MYH7c.5700G>T (p.Gln1900His)
14g.23413849C>GCA389034661MYH7c.5700G>C (p.Gln1900His)
14g.23413849C>TCA485616140MYH7c.5700G>A (p.Gln1900=)
14g.23413850T>ACA048008MYH7c.5699A>T (p.Gln1900Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23413850T>CCA389034662MYH7c.5699A>G (p.Gln1900Arg)
14g.23413850T>GCA389034663MYH7c.5699A>C (p.Gln1900Pro)
14g.23413850T=CA2123458480MYH7c.5699A= (p.Gln1900=)
14g.23413851G>ACA389034666MYH7c.5698C>T (p.Gln1900Ter)
14g.23413851G>CCA389034664MYH7c.5698C>G (p.Gln1900Glu)
14g.23413851G>TCA389034665MYH7c.5698C>A (p.Gln1900Lys)
14g.23413852C>ACA485616141MYH7c.5697G>T (p.Val1899=)
14g.23413852C=CA2123458486MYH7c.5697G= (p.Val1899=)
14g.23413852C>GCA485616142MYH7c.5697G>C (p.Val1899=)
14g.23413852C>TCA485616143MYH7c.5697G>A (p.Val1899=)
ClinVar dbSNP
14g.23413853A=CA2123458501MYH7c.5696T= (p.Val1899=)
14g.23413853A>CCA389034667MYH7c.5696T>G (p.Val1899Gly)
14g.23413853A>GCA016376MYH7c.5696T>C (p.Val1899Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23413853A>TCA389034668MYH7c.5696T>A (p.Val1899Glu)
14g.23413854C>ACA389034669MYH7c.5695G>T (p.Val1899Leu)
gnomAD v4
14g.23413854C>GCA389034670MYH7c.5695G>C (p.Val1899Leu)
gnomAD v4
14g.23413854C>TCA389034671MYH7c.5695G>A (p.Val1899Met)
ClinVar
14g.23413855C>ACA389034672MYH7c.5694G>T (p.Lys1898Asn)
14g.23413855C>GCA389034673MYH7c.5694G>C (p.Lys1898Asn)
gnomAD v4
14g.23413855C>TCA485616144MYH7c.5694G>A (p.Lys1898=)
gnomAD v4
14g.23413856T>ACA389034674MYH7c.5693A>T (p.Lys1898Met)
14g.23413856T>CCA389034675MYH7c.5693A>G (p.Lys1898Arg)
14g.23413856T>GCA389034676MYH7c.5693A>C (p.Lys1898Thr)
14g.23413857T>ACA389034677MYH7c.5692A>T (p.Lys1898Ter)
14g.23413857T>CCA389034678MYH7c.5692A>G (p.Lys1898Glu)
14g.23413857T>GCA389034679MYH7c.5692A>C (p.Lys1898Gln)
14g.23413858G>ACA485616145MYH7c.5691C>T (p.Arg1897=)
dbSNP gnomAD v2 gnomAD v4
14g.23413858G>CCA485616146MYH7c.5691C>G (p.Arg1897=)
14g.23413858G=CA2123458502MYH7c.5691C= (p.Arg1897=)
14g.23413858G>TCA485616147MYH7c.5691C>A (p.Arg1897=)
14g.23413859C>ACA389034681MYH7c.5690G>T (p.Arg1897Leu)
ClinVar COSMIC
14g.23413859C=CA2123458508MYH7c.5690G= (p.Arg1897=)
14g.23413859C>GCA389034680MYH7c.5690G>C (p.Arg1897Pro)
14g.23413859C>TCA016369MYH7c.5690G>A (p.Arg1897His)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23413860G>ACA047983MYH7c.5689C>T (p.Arg1897Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413860G>CCA389034682MYH7c.5689C>G (p.Arg1897Gly)
14g.23413860G=CA2123458522MYH7c.5689C= (p.Arg1897=)
14g.23413860G>TCA389034683MYH7c.5689C>A (p.Arg1897Ser)
14g.23413861G>ACA485616148MYH7c.5688C>T (p.Phe1896=)
14g.23413861G>CCA389034684MYH7c.5688C>G (p.Phe1896Leu)
dbSNP
14g.23413861G=CA2123458530MYH7c.5688C= (p.Phe1896=)
14g.23413861G>TCA389034685MYH7c.5688C>A (p.Phe1896Leu)
14g.23413862A=CA2123458541MYH7c.5687T= (p.Phe1896=)
14g.23413862A>CCA389034686MYH7c.5687T>G (p.Phe1896Cys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23413862A>GCA047967MYH7c.5687T>C (p.Phe1896Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23413862A>TCA389034687MYH7c.5687T>A (p.Phe1896Tyr)
14g.23413863A>CCA389034688MYH7c.5686T>G (p.Phe1896Val)
14g.23413863A>GCA389034689MYH7c.5686T>C (p.Phe1896Leu)
ClinVar gnomAD v4
14g.23413863A>TCA389034690MYH7c.5686T>A (p.Phe1896Ile)
14g.23413864C>ACA389034691MYH7c.5685G>T (p.Lys1895Asn)
14g.23413864C>GCA389034692MYH7c.5685G>C (p.Lys1895Asn)
14g.23413864C>TCA485616149MYH7c.5685G>A (p.Lys1895=)
14g.23413865T>ACA389034693MYH7c.5684A>T (p.Lys1895Met)
14g.23413865T>CCA257807584MYH7c.5684A>G (p.Lys1895Arg)
ClinVar dbSNP
14g.23413865T>GCA389034694MYH7c.5684A>C (p.Lys1895Thr)
14g.23413865T=CA2123458549MYH7c.5684A= (p.Lys1895=)
14g.23413866T>ACA389034695MYH7c.5683A>T (p.Lys1895Ter)
14g.23413866T>CCA389034696MYH7c.5683A>G (p.Lys1895Glu)
gnomAD v4
14g.23413866T>GCA389034697MYH7c.5683A>C (p.Lys1895Gln)
14g.23413867G>ACA485616150MYH7c.5682C>T (p.Ser1894=)
COSMIC
14g.23413867G>CCA485616152MYH7c.5682C>G (p.Ser1894=)
14g.23413867G>TCA485616151MYH7c.5682C>A (p.Ser1894=)
14g.23413868G>ACA389034698MYH7c.5681C>T (p.Ser1894Phe)
14g.23413868G>CCA389034700MYH7c.5681C>G (p.Ser1894Cys)
14g.23413868G>TCA389034699MYH7c.5681C>A (p.Ser1894Tyr)
14g.23413869A=CA2123458602MYH7c.5680T= (p.Ser1894=)
14g.23413869A>CCA389034701MYH7c.5680T>G (p.Ser1894Ala)
14g.23413869A>GCA389034703MYH7c.5680T>C (p.Ser1894Pro)
ClinVar dbSNP
14g.23413869A>TCA389034702MYH7c.5680T>A (p.Ser1894Thr)
14g.23413870C>ACA485616153MYH7c.5679G>T (p.Leu1893=)
14g.23413870C=CA2123458613MYH7c.5679G= (p.Leu1893=)
14g.23413870C>GCA485616154MYH7c.5679G>C (p.Leu1893=)
ClinVar dbSNP
14g.23413870C>TCA485616155MYH7c.5679G>A (p.Leu1893=)
14g.23413871A>CCA389034704MYH7c.5678T>G (p.Leu1893Arg)
14g.23413871A>GCA389034705MYH7c.5678T>C (p.Leu1893Pro)
14g.23413871A>TCA389034706MYH7c.5678T>A (p.Leu1893Gln)
14g.23413872G>ACA485616156MYH7c.5677C>T (p.Leu1893=)
14g.23413872G>CCA389034707MYH7c.5677C>G (p.Leu1893Val)
14g.23413872G>TCA389034708MYH7c.5677C>A (p.Leu1893Met)
14g.23413873G>ACA485616157MYH7c.5676C>T (p.Asn1892=)
ClinVar dbSNP gnomAD v4 COSMIC
14g.23413873G>CCA389034709MYH7c.5676C>G (p.Asn1892Lys)
14g.23413873G=CA2123458622MYH7c.5676C= (p.Asn1892=)
14g.23413873G>TCA389034710MYH7c.5676C>A (p.Asn1892Lys)
ClinVar dbSNP
14g.23413874T>ACA389034711MYH7c.5675A>T (p.Asn1892Ile)
14g.23413874T>CCA389034712MYH7c.5675A>G (p.Asn1892Ser)
14g.23413874T>GCA389034713MYH7c.5675A>C (p.Asn1892Thr)
14g.23413875T>ACA389034714MYH7c.5674A>T (p.Asn1892Tyr)
14g.23413875T>CCA389034715MYH7c.5674A>G (p.Asn1892Asp)
14g.23413875T>GCA389034716MYH7c.5674A>C (p.Asn1892His)
14g.23413876G>ACA485616158MYH7c.5673C>T (p.Thr1891=)
14g.23413876G>CCA485616159MYH7c.5673C>G (p.Thr1891=)
14g.23413876G>TCA485616160MYH7c.5673C>A (p.Thr1891=)
14g.23413877G>ACA389034717MYH7c.5672C>T (p.Thr1891Ile)
ClinVar dbSNP gnomAD v4
14g.23413877G>CCA389034719MYH7c.5672C>G (p.Thr1891Ser)
ClinVar
14g.23413877G>TCA389034718MYH7c.5672C>A (p.Thr1891Asn)
14g.23413878T>ACA389034720MYH7c.5671A>T (p.Thr1891Ser)
14g.23413878T>CCA389034721MYH7c.5671A>G (p.Thr1891Ala)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23413878T>GCA389034722MYH7c.5671A>C (p.Thr1891Pro)
14g.23413878T=CA2123458627MYH7c.5671A= (p.Thr1891=)
14g.23413879G>ACA485616161MYH7c.5670C>T (p.Asn1890=)
14g.23413879G>CCA389034723MYH7c.5670C>G (p.Asn1890Lys)
14g.23413879G>TCA389034724MYH7c.5670C>A (p.Asn1890Lys)
14g.23413880T>ACA389034725MYH7c.5669A>T (p.Asn1890Ile)
14g.23413880T>CCA389034726MYH7c.5669A>G (p.Asn1890Ser)
dbSNP gnomAD v3 gnomAD v4
14g.23413880T>GCA389034727MYH7c.5669A>C (p.Asn1890Thr)
14g.23413880T=CA2123458634MYH7c.5669A= (p.Asn1890=)
14g.23413881T>ACA389034728MYH7c.5668A>T (p.Asn1890Tyr)
gnomAD v4
14g.23413881T>CCA389034729MYH7c.5668A>G (p.Asn1890Asp)
gnomAD v4
14g.23413881T>GCA389034730MYH7c.5668A>C (p.Asn1890His)
14g.23413882G>ACA485616162MYH7c.5667C>T (p.Ala1889=)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23413882G>CCA485616163MYH7c.5667C>G (p.Ala1889=)
14g.23413882G=CA2123458645MYH7c.5667C= (p.Ala1889=)
14g.23413882G>TCA485616164MYH7c.5667C>A (p.Ala1889=)
14g.23413883G>ACA389034733MYH7c.5666C>T (p.Ala1889Val)
dbSNP gnomAD v2 gnomAD v4
14g.23413883G>CCA389034732MYH7c.5666C>G (p.Ala1889Gly)
ClinVar gnomAD v4
14g.23413883G=CA2123458650MYH7c.5666C= (p.Ala1889=)
14g.23413883G>TCA389034731MYH7c.5666C>A (p.Ala1889Asp)
14g.23413884C>ACA389034736MYH7c.5665G>T (p.Ala1889Ser)
14g.23413884C>GCA389034734MYH7c.5665G>C (p.Ala1889Pro)
14g.23413884C>TCA389034735MYH7c.5665G>A (p.Ala1889Thr)
14g.23413885T>ACA389034737MYH7c.5664A>T (p.Gln1888His)
14g.23413885T>CCA047949MYH7c.5664A>G (p.Gln1888=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413885T>GCA389034738MYH7c.5664A>C (p.Gln1888His)
14g.23413885T=CA2123458656MYH7c.5664A= (p.Gln1888=)
14g.23413886T>ACA389034741MYH7c.5663A>T (p.Gln1888Leu)
14g.23413886T>CCA389034740MYH7c.5663A>G (p.Gln1888Arg)
14g.23413886T>GCA389034739MYH7c.5663A>C (p.Gln1888Pro)
14g.23413887delCA2800863482MYH7c.5662del (p.Gln1888LysfsTer?)
14g.23413887G>ACA389034742MYH7c.5662C>T (p.Gln1888Ter)
ClinVar dbSNP gnomAD v4
14g.23413887G>CCA389034743MYH7c.5662C>G (p.Gln1888Glu)
14g.23413887G>TCA389034744MYH7c.5662C>A (p.Gln1888Lys)
14g.23413888C>ACA389034745MYH7c.5661G>T (p.Glu1887Asp)
COSMIC
14g.23413888C=CA2123458670MYH7c.5661G= (p.Glu1887=)
14g.23413888C>GCA389034746MYH7c.5661G>C (p.Glu1887Asp)
14g.23413888C>TCA016365MYH7c.5661G>A (p.Glu1887=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413889T>ACA389034747MYH7c.5660A>T (p.Glu1887Val)
14g.23413889T>CCA016357MYH7c.5660A>G (p.Glu1887Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413889T>GCA389034748MYH7c.5660A>C (p.Glu1887Ala)
14g.23413889T=CA2123458676MYH7c.5660A= (p.Glu1887=)
14g.23413889_23413890delinsTCCA2123458682MYH7c.5659_5660delinsGA (p.Glu1887=)
14g.23413890C>ACA389034749MYH7c.5659G>T (p.Glu1887Ter)
ClinVar dbSNP
14g.23413890C>GCA389034750MYH7c.5659G>C (p.Glu1887Gln)
14g.23413890C>TCA389034751MYH7c.5659G>A (p.Glu1887Lys)
gnomAD v4
14g.23413891delCA016354MYH7c.5659del (p.Glu1887SerfsTer?)
ClinVar dbSNP
14g.23413891C>ACA389034752MYH7c.5658G>T (p.Glu1886Asp)
14g.23413891C>GCA389034753MYH7c.5658G>C (p.Glu1886Asp)
14g.23413891C>TCA485616165MYH7c.5658G>A (p.Glu1886=)
gnomAD v4
14g.23413892T>ACA389034754MYH7c.5657A>T (p.Glu1886Val)
ClinVar dbSNP
14g.23413892T>CCA389034755MYH7c.5657A>G (p.Glu1886Gly)
dbSNP gnomAD v2 gnomAD v4
14g.23413892T>GCA389034756MYH7c.5657A>C (p.Glu1886Ala)
14g.23413892T=CA2123458695MYH7c.5657A= (p.Glu1886=)
14g.23413893C>ACA389034757MYH7c.5656G>T (p.Glu1886Ter)
14g.23413893C>GCA389034758MYH7c.5656G>C (p.Glu1886Gln)
14g.23413893C>TCA389034759MYH7c.5656G>A (p.Glu1886Lys)
gnomAD v4
14g.23413895_23414007delCA2800863485MYH7c.5655+2_5656del
14g.23413894C>ACA389034761MYH7c.5656-1G>T (n.5656-1G>T)
14g.23413894C=CA2123458698MYH7c.5656-1G= (n.5656-1G=)
14g.23413894C>GCA257807650MYH7c.5656-1G>C (n.5656-1G>C)
dbSNP gnomAD v3 gnomAD v4
14g.23413894C>TCA389034760MYH7c.5656-1G>A (n.5656-1G>A)
gnomAD v4 COSMIC
14g.23413895T>ACA389034762MYH7c.5656-2A>T (n.5656-2A>T)
14g.23413895T>CCA389034763MYH7c.5656-2A>G (n.5656-2A>G)
14g.23413895T>GCA257807666MYH7c.5656-2A>C (n.5656-2A>C)
dbSNP
14g.23413895T=CA2123458706MYH7c.5656-2A= (n.5656-2A=)
14g.23413897C>ACA2624230126MYH7c.5656-4G>T (n.5656-4G>T)
gnomAD v4
14g.23413897C=CA2123458716MYH7c.5656-4G= (n.5656-4G=)
14g.23413897C>GCA016341MYH7c.5656-4G>C (n.5656-4G>C)
ClinVar dbSNP gnomAD v4
14g.23413897C>TCA047894MYH7c.5656-4G>A (n.5656-4G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413898G>ACA047902MYH7c.5656-5C>T (n.5656-5C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23413898G=CA2123458724MYH7c.5656-5C= (n.5656-5C=)
14g.23413899G=CA2123458731MYH7c.5656-6C= (n.5656-6C=)
14g.23413899G>TCA612936598MYH7c.5656-6C>A (n.5656-6C>A)
ClinVar dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched