| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.153725687G>T | CA415098821 | ABCD1 | c.421G>T (p.Ala141Ser) n.837G>T | dbSNP |
| X | g.153725687G>A | CA278381 | ABCD1 | c.421G>A (p.Ala141Thr) n.837G>A | ClinVar dbSNP COSMIC |
| X | g.153725687G= | CA2466451018 | ABCD1 | c.421G= (p.Ala141=) n.837G= | dbSNP |