| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.153725748C>T | CA415098948 | ABCD1 | c.482C>T (p.Ser161Leu) n.898C>T | dbSNP |
| X | g.153725748C>A | CA415098947 | ABCD1 | c.482C>A (p.Ser161Ter) n.898C>A | ClinVar dbSNP |
| X | g.153725748C>G | CA337233997 | ABCD1 | c.482C>G (p.Ser161Trp) n.898C>G | dbSNP gnomAD v4 |