| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.55151856C>A | CA051933 | TNNI3 | c.611G>T (p.Arg204Leu) c.644G>T (p.Arg215Leu) n.610G>T c.536G>T (p.Arg179Leu) n.439G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 19 | g.55151856C>T | CA022060 | TNNI3 | c.611G>A (p.Arg204His) c.644G>A (p.Arg215His) n.610G>A c.536G>A (p.Arg179His) n.439G>A | ClinVar dbSNP gnomAD v4 |