P167S (p.Pro167Ser) variant of VPS35 (Q96QK1)
P167S (p.Pro167Ser) in VPS35 (Q96QK1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
P167S (p.Pro167Ser) variant details
- p.Pro167Ser
- NCI-TCGA Cosmic COSV1001
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.359
- REVEL 0.10
- CADD 20.80
- PolyPhen-2 0.00
- SIFT 0.85
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available