| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.55151910C>T | CA021907 | TNNI3 | c.557G>A (p.Arg186Gln) c.590G>A (p.Arg197Gln) n.556G>A c.482G>A (p.Arg161Gln) n.385G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 19 | g.55151910C= | CA2343272659 | TNNI3 | c.557G= (p.Arg186=) c.590G= (p.Arg197=) n.556G= c.482G= (p.Arg161=) n.385G= | dbSNP |