F29L (p.Phe29Leu) variant of SLC2A4 (P14672)
F29L (p.Phe29Leu) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data and structural context.
F29L (p.Phe29Leu) variant details
- p.Phe29Leu
- TOPMed rs1157269708
- gnomAD rs1157269708
- Missense
- Variant Prioritization Score for Impact Estimate 0.46
- REVEL 0.36
- CADD 22.50
- PolyPhen-2 0.02
- SIFT 0.38
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available