| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.55151899C>A | CA021939 | TNNI3 | c.568G>T (p.Asp190Tyr) c.601G>T (p.Asp201Tyr) n.567G>T c.493G>T (p.Asp165Tyr) n.396G>T | ClinVar dbSNP |
| 19 | g.55151899C= | CA2343272647 | TNNI3 | c.568G= (p.Asp190=) c.601G= (p.Asp201=) n.567G= c.493G= (p.Asp165=) n.396G= | dbSNP |