F5L (p.Phe5Leu) variant of SLC2A4 (P14672)
F5L (p.Phe5Leu) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data and structural context.
F5L (p.Phe5Leu) variant details
- p.Phe5Leu
- ExAC rs768920197
- TOPMed rs768920197
- gnomAD rs768920197
- Missense
- Variant Prioritization Score for Impact Estimate 0.406
- REVEL 0.29
- MetaLR 0.27
- MetaSVM -0.90
- CADD 25.10
- PolyPhen-2 0.00
- SIFT 0.06
- Most common in the East Asian population (allele frequency 5.2e-05)
- Structural context available