Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23431468C>T | CA016781 | MYH7 | c.746G>A (p.Arg249Gln) n.852G>A | ClinVar dbSNP gnomAD v4 COSMIC |
14 | g.23431468C>A | CA389052134 | MYH7 | c.746G>T (p.Arg249Leu) n.852G>T | ClinVar dbSNP |
14 | g.23431468C= | CA2123451619 | MYH7 | c.746G= (p.Arg249=) n.852G= | dbSNP |
14 | g.23431468C>G | CA389052135 | MYH7 | c.746G>C (p.Arg249Pro) n.852G>C | ClinVar dbSNP |