W117L (p.Trp117Leu) variant of SLC2A2 (P11168)
W117L (p.Trp117Leu) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
W117L (p.Trp117Leu) variant details
- p.Trp117Leu
- Ensembl rs2108256352
- Missense
- Variant Prioritization Score for Impact Estimate 0.225
- REVEL 0.14
- CADD 13.90
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the East Asian population (allele frequency 5e-05)
- Structural context available