R33G (p.Arg33Gly) variant of MOG (Q16653)
R33G (p.Arg33Gly) in MOG (Q16653) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
R33G (p.Arg33Gly) variant details
- p.Arg33Gly
- gnomAD rs1186928850
- Missense
- Variant Prioritization Score for Impact Estimate 0.292
- REVEL 0.19
- CADD 22.60
- PolyPhen-2 0.32
- SIFT 0.02
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available