G266R (p.Gly266Arg) variant of ATP1A3 (P13637)
G266R (p.Gly266Arg) in ATP1A3 (P13637) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.75 / 1. The record also includes population frequency data and structural context.
G266R (p.Gly266Arg) variant details
- p.Gly266Arg
- gnomAD rs2075274098
- Missense
- Variant Prioritization Score for Impact Estimate 0.752
- CADD 24.50
- Most common in the Ashkenazi Jewish population (allele frequency 0.00029)
- Structural context available