Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23396316_23396350delCA2624246239MYH6c.2366_2400del (p.Arg789HisfsTer2)
gnomAD v4
14g.23396329C>ACA389016189MYH6c.2384G>T (p.Arg795Leu)
14g.23396329C=CA2123417897MYH6c.2384G= (p.Arg795=)
14g.23396329C>GCA389016190MYH6c.2384G>C (p.Arg795Pro)
gnomAD v4
14g.23396329C>TCA123764MYH6c.2384G>A (p.Arg795Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23396330G>ACA7115483MYH6c.2383C>T (p.Arg795Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23396330G>CCA389016194MYH6c.2383C>G (p.Arg795Gly)
14g.23396330G=CA2123417903MYH6c.2383C= (p.Arg795=)
14g.23396330G>TCA485609947MYH6c.2383C>A (p.Arg795=)
gnomAD v4
14g.23396331G>ACA485609948MYH6c.2382C>T (p.Ala794=)
14g.23396331G>CCA485609949MYH6c.2382C>G (p.Ala794=)
14g.23396331G>TCA485609950MYH6c.2382C>A (p.Ala794=)
14g.23396332G>ACA389016197MYH6c.2381C>T (p.Ala794Val)
gnomAD v4
14g.23396332G>CCA389016198MYH6c.2381C>G (p.Ala794Gly)
14g.23396332G>TCA389016200MYH6c.2381C>A (p.Ala794Asp)
14g.23396333C>ACA389016202MYH6c.2380G>T (p.Ala794Ser)
14g.23396333C>GCA389016203MYH6c.2380G>C (p.Ala794Pro)
14g.23396333C>TCA389016205MYH6c.2380G>A (p.Ala794Thr)
14g.23396334T>ACA389016209MYH6c.2379A>T (p.Gln793His)
14g.23396334T>CCA7115484MYH6c.2379A>G (p.Gln793=)
ClinVar dbSNP ExAC gnomAD v4 COSMIC
14g.23396334T>GCA389016207MYH6c.2379A>C (p.Gln793His)
14g.23396334T=CA2123417911MYH6c.2379A= (p.Gln793=)
14g.23396335T>ACA389016212MYH6c.2378A>T (p.Gln793Leu)
14g.23396335T>CCA389016213MYH6c.2378A>G (p.Gln793Arg)
14g.23396335T>GCA389016214MYH6c.2378A>C (p.Gln793Pro)
14g.23396336G>ACA389016217MYH6c.2377C>T (p.Gln793Ter)
gnomAD v4
14g.23396336G>CCA389016218MYH6c.2377C>G (p.Gln793Glu)
14g.23396336G>TCA389016220MYH6c.2377C>A (p.Gln793Lys)
gnomAD v4
14g.23396337G>ACA485609955MYH6c.2376C>T (p.Ala792=)
dbSNP
14g.23396337G>CCA485609954MYH6c.2376C>G (p.Ala792=)
14g.23396337G=CA2123417915MYH6c.2376C= (p.Ala792=)
14g.23396337G>TCA485609953MYH6c.2376C>A (p.Ala792=)
14g.23396338G>ACA389016222MYH6c.2375C>T (p.Ala792Val)
14g.23396338G>CCA389016224MYH6c.2375C>G (p.Ala792Gly)
14g.23396338G>TCA389016223MYH6c.2375C>A (p.Ala792Asp)
14g.23396339C>ACA389016225MYH6c.2374G>T (p.Ala792Ser)
14g.23396339C>GCA389016227MYH6c.2374G>C (p.Ala792Pro)
14g.23396339C>TCA389016229MYH6c.2374G>A (p.Ala792Thr)
ClinVar
14g.23396340C>ACA389016231MYH6c.2373G>T (p.Gln791His)
dbSNP
14g.23396340C=CA2123417918MYH6c.2373G= (p.Gln791=)
14g.23396340C>GCA389016232MYH6c.2373G>C (p.Gln791His)
14g.23396340C>TCA485609958MYH6c.2373G>A (p.Gln791=)
14g.23396341T>ACA389016234MYH6c.2372A>T (p.Gln791Leu)
14g.23396341T>CCA389016236MYH6c.2372A>G (p.Gln791Arg)
gnomAD v4
14g.23396341T>GCA389016238MYH6c.2372A>C (p.Gln791Pro)
14g.23396342G>ACA257789181MYH6c.2371C>T (p.Gln791Ter)
dbSNP gnomAD v2 gnomAD v4
14g.23396342G>CCA7115485MYH6c.2371C>G (p.Gln791Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23396342G=CA2123417924MYH6c.2371C= (p.Gln791=)
14g.23396342G>TCA389016241MYH6c.2371C>A (p.Gln791Lys)
14g.23396343C>ACA389016243MYH6c.2370G>T (p.Met790Ile)

Number of alleles fetched