| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.55154065G>C | CA021797 | TNNI3 | c.514C>G (p.His172Asp) c.547C>G (p.His183Asp) n.513C>G c.439C>G (p.His147Asp) n.342C>G | ClinVar dbSNP |
| 19 | g.55154065G>A | CA407440296 | TNNI3 | c.514C>T (p.His172Tyr) c.547C>T (p.His183Tyr) n.513C>T c.439C>T (p.His147Tyr) n.342C>T | ClinVar dbSNP |