| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.7334060A>G | CA121124 | STS | c.1316A>G (p.His439Arg) n.1556A>G c.1178A>G (p.His393Arg) c.1331A>G (p.His444Arg) c.1352A>G (p.His451Arg) | ClinVar dbSNP |
| X | g.7334060A= | CA2414192749 | STS | c.1316A= (p.His439=) n.1556A= c.1178A= (p.His393=) c.1331A= (p.His444=) c.1352A= (p.His451=) | dbSNP |