L77F (p.Leu77Phe) variant of SLC2A4 (P14672)
L77F (p.Leu77Phe) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data and structural context.
L77F (p.Leu77Phe) variant details
- p.Leu77Phe
- ExAC rs746297235
- gnomAD rs746297235
- Missense
- Variant Prioritization Score for Impact Estimate 0.569
- REVEL 0.43
- CADD 23.70
- PolyPhen-2 0.52
- SIFT 0.03
- Most common in the Finnish in Finland (FIN) population (allele frequency 5.6e-05)
- Structural context available