Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23425760C>G | CA012013 | MYH7 | c.2221G>C (p.Gly741Arg) n.2327G>C | ClinVar dbSNP gnomAD v4 |
14 | g.23425760C>A | CA012022 | MYH7 | c.2221G>T (p.Gly741Trp) n.2327G>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
14 | g.23425760C>T | CA012004 | MYH7 | c.2221G>A (p.Gly741Arg) n.2327G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |