Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.153743046G>A | CA10550327 | ABCD1 | c.1840G>A (p.Gly614Ser) n.2312G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.153743046G>T | CA415116182 | ABCD1 | c.1840G>T (p.Gly614Cys) n.2312G>T | dbSNP gnomAD v4 |
X | g.153743046G= | CA2466457544 | ABCD1 | c.1840G= (p.Gly614=) n.2312G= | dbSNP |