Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.31525347T>C | CA224926 | SRD5A2 | c.*849A>G (n.*849A>G) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.31525347T= | CA1242195612 | SRD5A2 | c.*849A= (n.*849A=) | dbSNP |
2 | g.31525347T>A | CA425564172 | SRD5A2 | c.*849A>T (n.*849A>T) | dbSNP |
2 | g.31525347T>G | CA425564173 | SRD5A2 | c.*849A>C (n.*849A>C) | dbSNP |