R16W (p.Arg16Trp) variant of RP2 (Protein XRP2)
R16W (p.Arg16Trp) in RP2 (Protein XRP2) 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 0.22 / 1. The record also includes population frequency data and structural context.
R16W (p.Arg16Trp) variant details
- p.Arg16Trp
- NCI-TCGA Cosmic COSV5446
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.218
- REVEL 0.15
- CADD 19.50
- PolyPhen-2 0.06
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available