A71S (p.Ala71Ser) variant of HSD3B2 (P26439)
A71S (p.Ala71Ser) in HSD3B2 (P26439) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A71S (p.Ala71Ser) variant details
- p.Ala71Ser
- NCI-TCGA Cosmic COSV6559
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available