| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.149482894C>G | CA255270 | IDS | c.1505G>C (p.Trp502Ser) c.872G>C (p.Trp291Ser) c.1235G>C (p.Trp412Ser) | ClinVar dbSNP |
| X | g.149482894C>T | CA414517946 | IDS | c.1505G>A (p.Trp502Ter) c.872G>A (p.Trp291Ter) c.1235G>A (p.Trp412Ter) | ClinVar dbSNP |
| X | g.149482894C= | CA2465003963 | IDS | c.1505G= (p.Trp502=) c.872G= (p.Trp291=) c.1235G= (p.Trp412=) | dbSNP |