C11W (p.Cys11Trp) variant of SLC2A10 (O95528)
C11W (p.Cys11Trp) in SLC2A10 (O95528) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
C11W (p.Cys11Trp) variant details
- p.Cys11Trp
- TOPMed rs1431633342
- gnomAD rs1431633342
- Missense
- Variant Prioritization Score for Impact Estimate 0.441
- REVEL 0.52
- CADD 26.10
- PolyPhen-2 0.96
- SIFT 0.00
- Population evidence available
- Structural context available