| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.55151892C>G | CA021964 | TNNI3 | c.575G>C (p.Arg192Pro) c.608G>C (p.Arg203Pro) n.574G>C c.500G>C (p.Arg167Pro) n.403G>C | ClinVar dbSNP |
| 19 | g.55151892C>T | CA021957 | TNNI3 | c.575G>A (p.Arg192His) c.608G>A (p.Arg203His) n.574G>A c.500G>A (p.Arg167His) n.403G>A | ClinVar dbSNP gnomAD v4 COSMIC |
| 19 | g.55151892C>A | CA021971 | TNNI3 | c.575G>T (p.Arg192Leu) c.608G>T (p.Arg203Leu) n.574G>T c.500G>T (p.Arg167Leu) n.403G>T | ClinVar dbSNP |