| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.153740189G>A | CA278404 | ABCD1 | c.1586G>A (p.Gly529Asp) n.589G>A n.2058G>A | ClinVar dbSNP |
| X | g.153740189G>T | CA415111642 | ABCD1 | c.1586G>T (p.Gly529Val) n.589G>T n.2058G>T | ClinVar dbSNP |
| X | g.153740189G= | CA2466456442 | ABCD1 | c.1586G= (p.Gly529=) n.589G= n.2058G= | dbSNP |