| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.149483135A>G | CA414518469 | IDS | c.1264T>C (p.Cys422Arg) c.631T>C (p.Cys211Arg) n.371T>C c.994T>C (p.Cys332Arg) | ClinVar dbSNP |
| X | g.149483135A>C | CA255274 | IDS | c.1264T>G (p.Cys422Gly) c.631T>G (p.Cys211Gly) n.371T>G c.994T>G (p.Cys332Gly) | ClinVar dbSNP |
| X | g.149483135A= | CA2465004061 | IDS | c.1264T= (p.Cys422=) c.631T= (p.Cys211=) n.371T= c.994T= (p.Cys332=) | dbSNP |