| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23425413G>A | CA485622927 | MYH7 | c.2292C>T (p.Phe764=) n.2398C>T | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23425413G>C | CA012091 | MYH7 | c.2292C>G (p.Phe764Leu) n.2398C>G | ClinVar dbSNP |
| 14 | g.23425413G= | CA2123457754 | MYH7 | c.2292C= (p.Phe764=) n.2398C= | dbSNP |