| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.55154094C>T | CA021744 | TNNI3 | c.485G>A (p.Arg162Gln) c.518G>A (p.Arg173Gln) n.484G>A c.410G>A (p.Arg137Gln) n.313G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 19 | g.55154094C>A | CA407440359 | TNNI3 | c.485G>T (p.Arg162Leu) c.518G>T (p.Arg173Leu) n.484G>T c.410G>T (p.Arg137Leu) n.313G>T | ClinVar dbSNP |
| 19 | g.55154094C>G | CA021749 | TNNI3 | c.485G>C (p.Arg162Pro) c.518G>C (p.Arg173Pro) n.484G>C c.410G>C (p.Arg137Pro) n.313G>C | ClinVar dbSNP |
| 19 | g.55154094C= | CA2343273750 | TNNI3 | c.485G= (p.Arg162=) c.518G= (p.Arg173=) n.484G= c.410G= (p.Arg137=) n.313G= | dbSNP |