Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.153725754G>A | CA16043184 | ABCD1 | c.488G>A (p.Arg163His) n.904G>A | ClinVar dbSNP gnomAD v4 |
X | g.153725754G>C | CA415098961 | ABCD1 | c.488G>C (p.Arg163Pro) n.904G>C | ClinVar dbSNP |
X | g.153725754G>T | CA415098960 | ABCD1 | c.488G>T (p.Arg163Leu) n.904G>T | ClinVar dbSNP gnomAD v4 |