| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.55151881C>T | CA022006 | TNNI3 | c.586G>A (p.Asp196Asn) c.619G>A (p.Asp207Asn) n.585G>A c.511G>A (p.Asp171Asn) n.414G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.55151881C>A | CA022012 | TNNI3 | c.586G>T (p.Asp196Tyr) c.619G>T (p.Asp207Tyr) n.585G>T c.511G>T (p.Asp171Tyr) n.414G>T | ClinVar dbSNP gnomAD v4 |