| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.153743008G>A | CA278410 | ABCD1 | c.1802G>A (p.Trp601Ter) n.2274G>A | ClinVar dbSNP |
| X | g.153743008G= | CA2466457522 | ABCD1 | c.1802G= (p.Trp601=) n.2274G= | dbSNP |
| X | g.153743008G>C | CA415115754 | ABCD1 | c.1802G>C (p.Trp601Ser) n.2274G>C | ClinVar dbSNP |