R16Q (p.Arg16Gln) variant of ARAF (P10398)
R16Q (p.Arg16Gln) in ARAF (P10398) 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 0.51 / 1. The record also includes population frequency data, experimental measurements, and structural context.
R16Q (p.Arg16Gln) variant details
- p.Arg16Gln
- rs765492001
- ExAC rs765492001
- gnomAD rs765492001
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.507
- REVEL 0.37
- CADD 24.80
- PolyPhen-2 0.46
- SIFT 0.02
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the South Asian population (allele frequency 3.9e-05)
- Structural context available
- ARAF Raf-like Ras-binding domain domainome 1.0: score 0.0001