G4V (p.Gly4Val) variant of SLC2A4 (P14672)
G4V (p.Gly4Val) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data and structural context.
G4V (p.Gly4Val) variant details
- p.Gly4Val
- ExAC rs770994699
- TOPMed rs770994699
- gnomAD rs770994699
- Missense
- Variant Prioritization Score for Impact Estimate 0.508
- REVEL 0.41
- MetaLR 0.25
- MetaSVM -0.79
- CADD 24.40
- PolyPhen-2 0.05
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available