| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23425346G>A | CA012232 | MYH7 | c.2359C>T (p.Arg787Cys) n.2465C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425346G= | CA2123457529 | MYH7 | c.2359C= (p.Arg787=) n.2465C= | dbSNP |
| 14 | g.23425346G>C | CA389048581 | MYH7 | c.2359C>G (p.Arg787Gly) n.2465C>G | ClinVar dbSNP gnomAD v4 |