| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23415195C>G | CA389035733 | MYH7 | c.5359G>C (p.Glu1787Gln) | ClinVar dbSNP |
| 14 | g.23415195C= | CA2123462409 | MYH7 | c.5359G= (p.Glu1787=) | dbSNP |
| 14 | g.23415195C>T | CA389035734 | MYH7 | c.5359G>A (p.Glu1787Lys) | ClinVar dbSNP COSMIC |