| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.153725612G>A | CA278414 | ABCD1 | c.346G>A (p.Gly116Arg) n.762G>A | ClinVar dbSNP |
| X | g.153725612G>C | CA415098668 | ABCD1 | c.346G>C (p.Gly116Arg) n.762G>C | ClinVar dbSNP |
| X | g.153725612G>T | CA415098669 | ABCD1 | c.346G>T (p.Gly116Ter) n.762G>T | ClinVar dbSNP gnomAD v4 |
| X | g.153725612G= | CA2466450985 | ABCD1 | c.346G= (p.Gly116=) n.762G= | dbSNP |