| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.7334066G>A | CA121121 | STS | c.1322G>A (p.Cys441Tyr) n.1562G>A c.1184G>A (p.Cys395Tyr) c.1337G>A (p.Cys446Tyr) c.1358G>A (p.Cys453Tyr) | ClinVar dbSNP |
| X | g.7334066G= | CA2414192752 | STS | c.1322G= (p.Cys441=) n.1562G= c.1184G= (p.Cys395=) c.1337G= (p.Cys446=) c.1358G= (p.Cys453=) | dbSNP |