F51V (p.Phe51Val) variant of SPINK5 (Q9NQ38)
F51V (p.Phe51Val) in SPINK5 (Q9NQ38) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F51V (p.Phe51Val) variant details
- p.Phe51Val
- NCI-TCGA Cosmic COSV9980
- cosmic curated COSV99807
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available