G119A (p.Gly119Ala) variant of SLC2A2 (P11168)
G119A (p.Gly119Ala) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data and structural context.
G119A (p.Gly119Ala) variant details
- p.Gly119Ala
- ExAC rs746632604
- TOPMed rs746632604
- gnomAD rs746632604
- Missense
- Variant Prioritization Score for Impact Estimate 0.503
- REVEL 0.37
- CADD 16.00
- PolyPhen-2 0.01
- SIFT 1.00
- Most common in the Non-Finnish European population (allele frequency 5.4e-06)
- Structural context available