| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23415155G>A | CA016070 | MYH7 | c.5399C>T (p.Ala1800Val) | ClinVar dbSNP |
| 14 | g.23415155G= | CA2123462210 | MYH7 | c.5399C= (p.Ala1800=) | dbSNP |
| 14 | g.23415155G>T | CA389035596 | MYH7 | c.5399C>A (p.Ala1800Asp) | dbSNP gnomAD v4 |