| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.55154148A>G | CA021654 | TNNI3 | c.431T>C (p.Leu144Pro) c.464T>C (p.Leu155Pro) n.430T>C n.439T>C c.356T>C (p.Leu119Pro) n.259T>C | ClinVar dbSNP |
| 19 | g.55154148A>T | CA021648 | TNNI3 | c.431T>A (p.Leu144Gln) c.464T>A (p.Leu155Gln) n.430T>A n.439T>A c.356T>A (p.Leu119Gln) n.259T>A | ClinVar dbSNP |