R17W (p.Arg17Trp) variant of PIK3R2 (O00459)
R17W (p.Arg17Trp) in PIK3R2 (O00459) 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 0.44 / 1. The record also includes population frequency data and structural context.
R17W (p.Arg17Trp) variant details
- p.Arg17Trp
- rs868385898
- NCI-TCGA Cosmic COSV5321
- cosmic curated COSV53217
- gnomAD rs868385898
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.436
- REVEL 0.16
- CADD 29.70
- PolyPhen-2 0.73
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available