Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23415082_23415093delCA2624231769MYH7c.5470_5481del (p.Asn1824_Glu1827del)
gnomAD v4
14g.23415089_23415101delCA2580610817MYH7c.5455_5467del (p.Val1819ArgfsTer15)
14g.23415088C>ACA485765953MYH7c.5466G>T (p.Leu1822=)
14g.23415088C>GCA485765954MYH7c.5466G>C (p.Leu1822=)
14g.23415088C>TCA485765956MYH7c.5466G>A (p.Leu1822=)
14g.23415089A>CCA389035277MYH7c.5465T>G (p.Leu1822Arg)
14g.23415089A>GCA389035282MYH7c.5465T>C (p.Leu1822Pro)
14g.23415089A>TCA389035280MYH7c.5465T>A (p.Leu1822Gln)
14g.23415090delCA2624231812MYH7c.5464del (p.Leu1822TrpfsTer16)
gnomAD v4
14g.23415090G>ACA485765959MYH7c.5464C>T (p.Leu1822=)
14g.23415090G>CCA389035285MYH7c.5464C>G (p.Leu1822Val)
14g.23415090G>TCA389035287MYH7c.5464C>A (p.Leu1822Met)
14g.23415091C>ACA389035290MYH7c.5463G>T (p.Glu1821Asp)
14g.23415091C>GCA389035291MYH7c.5463G>C (p.Glu1821Asp)
14g.23415091C>TCA485765965MYH7c.5463G>A (p.Glu1821=)
14g.23415092_23415093dupCA2624231820MYH7c.5462_5463dup (p.Leu1822SerfsTer17)
gnomAD v4
14g.23415092T>ACA389035294MYH7c.5462A>T (p.Glu1821Val)
14g.23415092T>CCA389035296MYH7c.5462A>G (p.Glu1821Gly)
14g.23415092T>GCA389035298MYH7c.5462A>C (p.Glu1821Ala)
14g.23415093C>ACA389035301MYH7c.5461G>T (p.Glu1821Ter)
14g.23415093C>GCA389035303MYH7c.5461G>C (p.Glu1821Gln)
14g.23415093C>TCA389035305MYH7c.5461G>A (p.Glu1821Lys)
gnomAD v4
14g.23415094C>ACA485765972MYH7c.5460G>T (p.Arg1820=)
14g.23415094C>GCA485765973MYH7c.5460G>C (p.Arg1820=)
ClinVar
14g.23415094C>TCA485765976MYH7c.5460G>A (p.Arg1820=)
gnomAD v4
14g.23415095C>ACA389035311MYH7c.5459G>T (p.Arg1820Leu)
14g.23415095C=CA2123461914MYH7c.5459G= (p.Arg1820=)
14g.23415095C>GCA389035309MYH7c.5459G>C (p.Arg1820Pro)
14g.23415095C>TCA046848MYH7c.5459G>A (p.Arg1820Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23415096G>ACA016126MYH7c.5458C>T (p.Arg1820Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415096G>CCA046829MYH7c.5458C>G (p.Arg1820Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415096G=CA2123461925MYH7c.5458C= (p.Arg1820=)
14g.23415096G>TCA485765981MYH7c.5458C>A (p.Arg1820=)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23415097C>ACA485765983MYH7c.5457G>T (p.Val1819=)
dbSNP gnomAD v2 gnomAD v4
14g.23415097C=CA2123461938MYH7c.5457G= (p.Val1819=)
14g.23415097C>GCA485765985MYH7c.5457G>C (p.Val1819=)
dbSNP
14g.23415097C>TCA485765986MYH7c.5457G>A (p.Val1819=)
14g.23415098A=CA2123461943MYH7c.5456T= (p.Val1819=)
14g.23415098A>CCA389035316MYH7c.5456T>G (p.Val1819Gly)
ClinVar dbSNP gnomAD v4
14g.23415098A>GCA389035318MYH7c.5456T>C (p.Val1819Ala)
14g.23415098A>TCA389035319MYH7c.5456T>A (p.Val1819Glu)
14g.23415099C>ACA389035322MYH7c.5455G>T (p.Val1819Leu)
gnomAD v4
14g.23415099C>GCA389035324MYH7c.5455G>C (p.Val1819Leu)
gnomAD v4
14g.23415099C>TCA389035326MYH7c.5455G>A (p.Val1819Met)
14g.23415100C>ACA485765993MYH7c.5454G>T (p.Arg1818=)
14g.23415100C>GCA485765995MYH7c.5454G>C (p.Arg1818=)
14g.23415100C>TCA485765997MYH7c.5454G>A (p.Arg1818=)
gnomAD v4
14g.23415101C>ACA389035328MYH7c.5453G>T (p.Arg1818Leu)
14g.23415101C=CA2123461956MYH7c.5453G= (p.Arg1818=)
14g.23415101C>GCA389035329MYH7c.5453G>C (p.Arg1818Pro)

Number of alleles fetched