| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.31580690G>A | CA16609845 | SRD5A2 | c.211C>T (p.Gln71Ter) c.27-46924C>T (n.27-46924C>T) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.31580690G= | CA1242221055 | SRD5A2 | c.211C= (p.Gln71=) c.27-46924C= (n.27-46924C=) | dbSNP |