| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23425372T>A | CA389048628 | MYH7 | c.2333A>T (p.Asp778Val) n.2439A>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23425372T>C | CA012133 | MYH7 | c.2333A>G (p.Asp778Gly) n.2439A>G | ClinVar dbSNP |
| 14 | g.23425372T= | CA2123457656 | MYH7 | c.2333A= (p.Asp778=) n.2439A= | dbSNP |