Chr Mutation (hg38) CAid Gene Transcript Linkouts
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=)
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)

Number of alleles fetched