S63G (p.Ser63Gly) variant of SLC2A2 (P11168)
S63G (p.Ser63Gly) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
S63G (p.Ser63Gly) variant details
- p.Ser63Gly
- Ensembl rs1716049094
- Missense
- Variant Prioritization Score for Impact Estimate 0.195
- REVEL 0.18
- CADD 12.30
- PolyPhen-2 0.00
- SIFT 0.37
- Most common in the East Asian population (allele frequency 5e-05)
- Structural context available