R36Q (p.Arg36Gln) variant of ARAF (P10398)
R36Q (p.Arg36Gln) in ARAF (P10398) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.80 / 1. The record also includes population frequency data, experimental measurements, and structural context.
R36Q (p.Arg36Gln) variant details
- p.Arg36Gln
- cosmic curated COSV10439
- Missense
- Variant Prioritization Score for Impact Estimate 0.801
- REVEL 0.86
- CADD 27.80
- PolyPhen-2 0.97
- SIFT 0.05
- Most common in the Ashkenazi Jewish population (allele frequency 5.2e-05)
- Structural context available
- ARAF Raf-like Ras-binding domain domainome 1.0: score -0.169