R19G (p.Arg19Gly) variant of SLC2A4 (P14672)
R19G (p.Arg19Gly) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
R19G (p.Arg19Gly) variant details
- p.Arg19Gly
- 1000Genomes rs139011011
- ESP rs139011011
- ExAC rs139011011
- TOPMed rs139011011
- Missense
- Variant Prioritization Score for Impact Estimate 0.229
- REVEL 0.08
- CADD 17.40
- PolyPhen-2 0.00
- SIFT 0.25
- Most common in the 1KG:GWD population (allele frequency 0.052)
- Structural context available