| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.55154146G>C | CA021660 | TNNI3 | c.433C>G (p.Arg145Gly) c.466C>G (p.Arg156Gly) n.432C>G n.441C>G c.358C>G (p.Arg120Gly) n.261C>G | ClinVar dbSNP gnomAD v4 |
| 19 | g.55154146G>A | CA021667 | TNNI3 | c.433C>T (p.Arg145Trp) c.466C>T (p.Arg156Trp) n.432C>T n.441C>T c.358C>T (p.Arg120Trp) n.261C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 19 | g.55154146G= | CA2343273777 | TNNI3 | c.433C= (p.Arg145=) c.466C= (p.Arg156=) n.432C= n.441C= c.358C= (p.Arg120=) n.261C= | dbSNP |
| 19 | g.55154146G>T | CA508989444 | TNNI3 | c.433C>A (p.Arg145=) c.466C>A (p.Arg156=) n.432C>A n.441C>A c.358C>A (p.Arg120=) n.261C>A | ClinVar dbSNP gnomAD v4 |