P9A (p.Pro9Ala) variant of SRD5A2 (P31213)
P9A (p.Pro9Ala) in SRD5A2 (P31213) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P9A (p.Pro9Ala) variant details
- p.Pro9Ala
- NCI-TCGA Cosmic COSV9925
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available