| 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 |
| 19 | g.55151881C>G | CA407439559 | TNNI3 | c.586G>C (p.Asp196His) c.619G>C (p.Asp207His) n.585G>C c.511G>C (p.Asp171His) n.414G>C | ClinVar dbSNP |
| 19 | g.55151881C= | CA2343272564 | TNNI3 | c.586G= (p.Asp196=) c.619G= (p.Asp207=) n.585G= c.511G= (p.Asp171=) n.414G= | dbSNP |