Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.31526225G>A | CA340064 | SRD5A2 | c.736C>T (p.Arg246Trp) c.514C>T (p.Arg172Trp) c.481C>T (p.Arg161Trp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.31526225G>T | CA425566641 | SRD5A2 | c.736C>A (p.Arg246=) c.514C>A (p.Arg172=) c.481C>A (p.Arg161=) | dbSNP gnomAD v4 |
2 | g.31526225G= | CA1242195945 | SRD5A2 | c.736C= (p.Arg246=) c.514C= (p.Arg172=) c.481C= (p.Arg161=) | dbSNP |