| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.153740618C>G | CA415112678 | ABCD1 | c.1679C>G (p.Pro560Arg) n.2151C>G | ClinVar dbSNP |
| X | g.153740618C>T | CA278408 | ABCD1 | c.1679C>T (p.Pro560Leu) n.2151C>T | ClinVar dbSNP gnomAD v4 |
| X | g.153740618C= | CA2466456607 | ABCD1 | c.1679C= (p.Pro560=) n.2151C= | dbSNP |