| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.55151917C>G | CA407439699 | TNNI3 | c.550G>C (p.Glu184Gln) c.583G>C (p.Glu195Gln) n.549G>C c.475G>C (p.Glu159Gln) n.378G>C | ClinVar dbSNP |
| 19 | g.55151917C>T | CA021885 | TNNI3 | c.550G>A (p.Glu184Lys) c.583G>A (p.Glu195Lys) n.549G>A c.475G>A (p.Glu159Lys) n.378G>A | ClinVar dbSNP |