F22L (p.Phe22Leu) variant of SLC2A2 (P11168)
F22L (p.Phe22Leu) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
F22L (p.Phe22Leu) variant details
- p.Phe22Leu
- ESP rs369781481
- TOPMed rs369781481
- gnomAD rs369781481
- Missense
- Variant Prioritization Score for Impact Estimate 0.319
- REVEL 0.26
- CADD 17.90
- PolyPhen-2 0.25
- SIFT 0.96
- Most common in the African/African-American population (allele frequency 7.2e-05)
- Structural context available