R66W (p.Arg66Trp) variant of ATXN2 (Ataxin-2)
R66W (p.Arg66Trp) in ATXN2 (Ataxin-2) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.68 / 1. The record also includes population frequency data.
R66W (p.Arg66Trp) variant details
- p.Arg66Trp
- Ensembl rs1350840606
- Missense
- Variant Prioritization Score for Impact Estimate 0.68
- CADD 22.80
- Most common in the African/African-American population (allele frequency 4.8e-05)