| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23426834G>T | CA389049378 | MYH7 | c.1987C>A (p.Arg663Ser) n.2093C>A | ClinVar dbSNP |
| 14 | g.23426834G>A | CA011543 | MYH7 | c.1987C>T (p.Arg663Cys) n.2093C>T | ClinVar dbSNP gnomAD v4 COSMIC |
| 14 | g.23426834G>C | CA389049377 | MYH7 | c.1987C>G (p.Arg663Gly) n.2093C>G | dbSNP |