| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.55154070C>T | CA021784 | TNNI3 | c.509G>A (p.Arg170Gln) c.542G>A (p.Arg181Gln) n.508G>A c.434G>A (p.Arg145Gln) n.337G>A | ClinVar dbSNP gnomAD v4 COSMIC |
| 19 | g.55154070C>G | CA407440303 | TNNI3 | c.509G>C (p.Arg170Pro) c.542G>C (p.Arg181Pro) n.508G>C c.434G>C (p.Arg145Pro) n.337G>C | ClinVar dbSNP |
| 19 | g.55154070C= | CA2343273734 | TNNI3 | c.509G= (p.Arg170=) c.542G= (p.Arg181=) n.508G= c.434G= (p.Arg145=) n.337G= | dbSNP |