P42S (p.Pro42Ser) variant of SRD5A2 (P31213)
P42S (p.Pro42Ser) in SRD5A2 (P31213) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
P42S (p.Pro42Ser) variant details
- p.Pro42Ser
- NCI-TCGA Cosmic COSV9925
- Variant assessed as somatic; moderate impact.
- Missense
- SIFT 0.19
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available