Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23431468C>TCA016781MYH7c.746G>A (p.Arg249Gln)
n.852G>A
ClinVar dbSNP gnomAD v4 COSMIC
14g.23431468C>ACA389052134MYH7c.746G>T (p.Arg249Leu)
n.852G>T
ClinVar dbSNP
14g.23431468C=CA2123451619MYH7c.746G= (p.Arg249=)
n.852G=
dbSNP
14g.23431468C>GCA389052135MYH7c.746G>C (p.Arg249Pro)
n.852G>C
ClinVar dbSNP

Number of alleles fetched