| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.55151851T>C | CA022079 | TNNI3 | c.616A>G (p.Lys206Glu) c.649A>G (p.Lys217Glu) n.615A>G c.541A>G (p.Lys181Glu) n.444A>G | ClinVar dbSNP |
| 19 | g.55151851T>G | CA022072 | TNNI3 | c.616A>C (p.Lys206Gln) c.649A>C (p.Lys217Gln) n.615A>C c.541A>C (p.Lys181Gln) n.444A>C | ClinVar dbSNP |
| 19 | g.55151851T>A | CA407439447 | TNNI3 | c.616A>T (p.Lys206Ter) c.649A>T (p.Lys217Ter) n.615A>T c.541A>T (p.Lys181Ter) n.444A>T | dbSNP |
| 19 | g.55151851T= | CA2343272459 | TNNI3 | c.616A= (p.Lys206=) c.649A= (p.Lys217=) n.615A= c.541A= (p.Lys181=) n.444A= | dbSNP |