| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23424817C>G | CA389047941 | MYH7 | c.2631G>C (p.Met877Ile) n.2737G>C | ClinVar dbSNP gnomAD v4 |
| 14 | g.23424817C>A | CA16609633 | MYH7 | c.2631G>T (p.Met877Ile) n.2737G>T | ClinVar dbSNP gnomAD v4 COSMIC |
| 14 | g.23424817C>T | CA389047943 | MYH7 | c.2631G>A (p.Met877Ile) n.2737G>A | ClinVar dbSNP |