Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.50210724C>ACA406946681MYH14c.359C>A (p.Ser120Ter)
c.-1932C>A (n.-1932C>A)
c.479C>A (p.Ser160Ter)
gnomAD v4
19g.50210724C=CA2340790068MYH14c.359C= (p.Ser120=)
c.-1932C= (n.-1932C=)
c.479C= (p.Ser160=)
19g.50210724C>GCA406946682MYH14c.359C>G (p.Ser120Trp)
c.-1932C>G (n.-1932C>G)
c.479C>G (p.Ser160Trp)
gnomAD v4
19g.50210724C>TCA252137MYH14c.359C>T (p.Ser120Leu)
c.-1932C>T (n.-1932C>T)
c.479C>T (p.Ser160Leu)
ClinVar dbSNP gnomAD v4
19g.50210725G>ACA508175280MYH14c.360G>A (p.Ser120=)
c.-1931G>A (n.-1931G>A)
c.480G>A (p.Ser160=)
dbSNP gnomAD v4
19g.50210725G>CCA508175281MYH14c.360G>C (p.Ser120=)
c.-1931G>C (n.-1931G>C)
c.480G>C (p.Ser160=)
gnomAD v4
19g.50210725G=CA2340790070MYH14c.360G= (p.Ser120=)
c.-1931G= (n.-1931G=)
c.480G= (p.Ser160=)
19g.50210725G>TCA508175282MYH14c.360G>T (p.Ser120=)
c.-1931G>T (n.-1931G>T)
c.480G>T (p.Ser160=)
gnomAD v4
19g.50210726delCA2586537518MYH14c.361del (p.Val121SerfsTer?)
c.-1930del (n.-1930del)
c.481del (p.Val161SerfsTer?)
gnomAD v4
19g.50210726G>ACA406946687MYH14c.361G>A (p.Val121Ile)
c.-1930G>A (n.-1930G>A)
c.481G>A (p.Val161Ile)
gnomAD v4
19g.50210726G>CCA406946689MYH14c.361G>C (p.Val121Leu)
c.-1930G>C (n.-1930G>C)
c.481G>C (p.Val161Leu)
19g.50210726G>TCA406946685MYH14c.361G>T (p.Val121Phe)
c.-1930G>T (n.-1930G>T)
c.481G>T (p.Val161Phe)
19g.50210727T>ACA406946691MYH14c.362T>A (p.Val121Asp)
c.-1929T>A (n.-1929T>A)
c.482T>A (p.Val161Asp)
19g.50210727T>CCA406946693MYH14c.362T>C (p.Val121Ala)
c.-1929T>C (n.-1929T>C)
c.482T>C (p.Val161Ala)
19g.50210727T>GCA406946696MYH14c.362T>G (p.Val121Gly)
c.-1929T>G (n.-1929T>G)
c.482T>G (p.Val161Gly)
19g.50210728C>ACA508175283MYH14c.363C>A (p.Val121=)
c.-1928C>A (n.-1928C>A)
c.483C>A (p.Val161=)
gnomAD v4 COSMIC COSMIC COSMIC
19g.50210728C>GCA508175284MYH14c.363C>G (p.Val121=)
c.-1928C>G (n.-1928C>G)
c.483C>G (p.Val161=)
gnomAD v4
19g.50210728C>TCA508175285MYH14c.363C>T (p.Val121=)
c.-1928C>T (n.-1928C>T)
c.483C>T (p.Val161=)
gnomAD v4
19g.50210729C>ACA406946697MYH14c.364C>A (p.Leu122Met)
c.-1927C>A (n.-1927C>A)
c.484C>A (p.Leu162Met)
gnomAD v4
19g.50210729C>GCA406946699MYH14c.364C>G (p.Leu122Val)
c.-1927C>G (n.-1927C>G)
c.484C>G (p.Leu162Val)
19g.50210729C>TCA508175286MYH14c.364C>T (p.Leu122=)
c.-1927C>T (n.-1927C>T)
c.484C>T (p.Leu162=)
gnomAD v4
19g.50210730T>ACA406946706MYH14c.365T>A (p.Leu122Gln)
c.-1926T>A (n.-1926T>A)
c.485T>A (p.Leu162Gln)
gnomAD v4
19g.50210730T>CCA406946702MYH14c.365T>C (p.Leu122Pro)
c.-1926T>C (n.-1926T>C)
c.485T>C (p.Leu162Pro)
dbSNP gnomAD v4
19g.50210730T>GCA406946704MYH14c.365T>G (p.Leu122Arg)
c.-1926T>G (n.-1926T>G)
c.485T>G (p.Leu162Arg)
19g.50210731G>ACA508175287MYH14c.366G>A (p.Leu122=)
c.-1925G>A (n.-1925G>A)
c.486G>A (p.Leu162=)
gnomAD v4
19g.50210731G>CCA508175288MYH14c.366G>C (p.Leu122=)
c.-1925G>C (n.-1925G>C)
c.486G>C (p.Leu162=)
19g.50210731G>TCA508175289MYH14c.366G>T (p.Leu122=)
c.-1925G>T (n.-1925G>T)
c.486G>T (p.Leu162=)
gnomAD v4
19g.50210732delCA2586537519MYH14c.367del (p.His123ThrfsTer?)
c.-1924del (n.-1924del)
c.487del (p.His163ThrfsTer?)
gnomAD v4
19g.50210732C>ACA406946708MYH14c.367C>A (p.His123Asn)
c.-1924C>A (n.-1924C>A)
c.487C>A (p.His163Asn)
gnomAD v4
19g.50210732C>GCA406946710MYH14c.367C>G (p.His123Asp)
c.-1924C>G (n.-1924C>G)
c.487C>G (p.His163Asp)
19g.50210732C>TCA406946712MYH14c.367C>T (p.His123Tyr)
c.-1924C>T (n.-1924C>T)
c.487C>T (p.His163Tyr)
gnomAD v4 COSMIC COSMIC COSMIC
19g.50210733A>CCA406946714MYH14c.368A>C (p.His123Pro)
c.-1923A>C (n.-1923A>C)
c.488A>C (p.His163Pro)
gnomAD v4
19g.50210733A>GCA406946716MYH14c.368A>G (p.His123Arg)
c.-1923A>G (n.-1923A>G)
c.488A>G (p.His163Arg)
19g.50210733A>TCA406946718MYH14c.368A>T (p.His123Leu)
c.-1923A>T (n.-1923A>T)
c.488A>T (p.His163Leu)
19g.50210734C>ACA406946720MYH14c.369C>A (p.His123Gln)
c.-1922C>A (n.-1922C>A)
c.489C>A (p.His163Gln)
gnomAD v4
19g.50210734C>GCA406946719MYH14c.369C>G (p.His123Gln)
c.-1922C>G (n.-1922C>G)
c.489C>G (p.His163Gln)
gnomAD v4
19g.50210734C>TCA508175290MYH14c.369C>T (p.His123=)
c.-1922C>T (n.-1922C>T)
c.489C>T (p.His163=)
gnomAD v4
19g.50210735A>CCA406946722MYH14c.370A>C (p.Asn124His)
c.-1921A>C (n.-1921A>C)
c.490A>C (p.Asn164His)
19g.50210735A>GCA406946723MYH14c.370A>G (p.Asn124Asp)
c.-1921A>G (n.-1921A>G)
c.490A>G (p.Asn164Asp)
gnomAD v4
19g.50210735A>TCA406946725MYH14c.370A>T (p.Asn124Tyr)
c.-1921A>T (n.-1921A>T)
c.490A>T (p.Asn164Tyr)
19g.50210736A=CA2340790071MYH14c.371A= (p.Asn124=)
c.-1920A= (n.-1920A=)
c.491A= (p.Asn164=)
19g.50210736A>CCA406946727MYH14c.371A>C (p.Asn124Thr)
c.-1920A>C (n.-1920A>C)
c.491A>C (p.Asn164Thr)
gnomAD v4
19g.50210736A>GCA406946729MYH14c.371A>G (p.Asn124Ser)
c.-1920A>G (n.-1920A>G)
c.491A>G (p.Asn164Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.50210736A>TCA406946730MYH14c.371A>T (p.Asn124Ile)
c.-1920A>T (n.-1920A>T)
c.491A>T (p.Asn164Ile)
19g.50210737C>ACA406946732MYH14c.372C>A (p.Asn124Lys)
c.-1919C>A (n.-1919C>A)
c.492C>A (p.Asn164Lys)
gnomAD v4
19g.50210737C=CA2340790079MYH14c.372C= (p.Asn124=)
c.-1919C= (n.-1919C=)
c.492C= (p.Asn164=)
19g.50210737C>GCA406946734MYH14c.372C>G (p.Asn124Lys)
c.-1919C>G (n.-1919C>G)
c.492C>G (p.Asn164Lys)
19g.50210737C>TCA508175291MYH14c.372C>T (p.Asn124=)
c.-1919C>T (n.-1919C>T)
c.492C>T (p.Asn164=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.50210738C>ACA406946736MYH14c.373C>A (p.Leu125Ile)
c.-1918C>A (n.-1918C>A)
c.493C>A (p.Leu165Ile)
gnomAD v4
19g.50210738C=CA2340790082MYH14c.373C= (p.Leu125=)
c.-1918C= (n.-1918C=)
c.493C= (p.Leu165=)

Number of alleles fetched