Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.31580823G>A | CA767788344 | SRD5A2 | c.78C>T (p.Tyr26=) c.27-47057C>T (n.27-47057C>T) | ClinVar dbSNP gnomAD v4 |
2 | g.31580823G>C | CA346599154 | SRD5A2 | c.78C>G (p.Tyr26Ter) c.27-47057C>G (n.27-47057C>G) | ClinVar dbSNP gnomAD v4 |