| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.55151888C>A | CA021989 | TNNI3 | c.579G>T (p.Lys193Asn) c.612G>T (p.Lys204Asn) n.578G>T c.504G>T (p.Lys168Asn) n.407G>T | ClinVar dbSNP |
| 19 | g.55151888C>G | CA021983 | TNNI3 | c.579G>C (p.Lys193Asn) c.612G>C (p.Lys204Asn) n.578G>C c.504G>C (p.Lys168Asn) n.407G>C | ClinVar dbSNP |
| 19 | g.55151888C= | CA2343272604 | TNNI3 | c.579G= (p.Lys193=) c.612G= (p.Lys204=) n.578G= c.504G= (p.Lys168=) n.407G= | dbSNP |