C11G (p.Cys11Gly) variant of SLC2A10 (O95528)
C11G (p.Cys11Gly) in SLC2A10 (O95528) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data and structural context.
C11G (p.Cys11Gly) variant details
- p.Cys11Gly
- TOPMed rs1168483717
- gnomAD rs1168483717
- Missense
- Variant Prioritization Score for Impact Estimate 0.555
- REVEL 0.59
- CADD 22.30
- PolyPhen-2 0.29
- SIFT 0.05
- Population evidence available
- Structural context available