G138E (p.Gly138Glu) variant of SLC2A2 (P11168)
G138E (p.Gly138Glu) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.77 / 1. The record also includes population frequency data and structural context.
G138E (p.Gly138Glu) variant details
- p.Gly138Glu
- gnomAD rs1300072764
- Missense
- Variant Prioritization Score for Impact Estimate 0.768
- REVEL 0.84
- CADD 25.20
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available