| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.55154115A>G | CA021714 | TNNI3 | c.464T>C (p.Met155Thr) c.497T>C (p.Met166Thr) n.463T>C n.472T>C c.389T>C (p.Met130Thr) n.292T>C | ClinVar dbSNP |
| 19 | g.55154115A= | CA2343273762 | TNNI3 | c.464T= (p.Met155=) c.497T= (p.Met166=) n.463T= n.472T= c.389T= (p.Met130=) n.292T= | dbSNP |