G66E (p.Gly66Glu) variant of SRD5A2 (P31213)
G66E (p.Gly66Glu) in SRD5A2 (P31213) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
G66E (p.Gly66Glu) variant details
- p.Gly66Glu
- NCI-TCGA Cosmic COSV5187
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.