G13E (p.Gly13Glu) variant of SLC2A4 (P14672)
G13E (p.Gly13Glu) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
G13E (p.Gly13Glu) variant details
- p.Gly13Glu
- ExAC rs755868694
- TOPMed rs755868694
- gnomAD rs755868694
- Missense
- Variant Prioritization Score for Impact Estimate 0.393
- REVEL 0.21
- MetaLR 0.21
- MetaSVM -0.90
- CADD 18.40
- PolyPhen-2 0.00
- SIFT 0.36
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available