G47S (p.Gly47Ser) variant of SLC2A2 (P11168)
G47S (p.Gly47Ser) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
G47S (p.Gly47Ser) variant details
- p.Gly47Ser
- Ensembl rs1159338702
- Missense
- Variant Prioritization Score for Impact Estimate 0.33
- REVEL 0.29
- CADD 21.70
- PolyPhen-2 0.65
- SIFT 0.10
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available