| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23425345C>T | CA012239 | MYH7 | c.2360G>A (p.Arg787His) n.2466G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23425345C>G | CA389048579 | MYH7 | c.2360G>C (p.Arg787Pro) n.2466G>C | ClinVar dbSNP |
| 14 | g.23425345C= | CA2123457518 | MYH7 | c.2360G= (p.Arg787=) n.2466G= | dbSNP |