R88W (p.Arg88Trp) variant of STAT2 (P52630)
R88W (p.Arg88Trp) in STAT2 (P52630) 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 0.37 / 1. The record also includes population frequency data and structural context.
R88W (p.Arg88Trp) variant details
- p.Arg88Trp
- NCI-TCGA Cosmic COSV5847
- cosmic curated COSV58477
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.371
- REVEL 0.45
- CADD 25.80
- PolyPhen-2 1.00
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available