D39G (p.Asp39Gly) variant of SLC2A10 (O95528)
D39G (p.Asp39Gly) in SLC2A10 (O95528) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data and structural context.
D39G (p.Asp39Gly) variant details
- p.Asp39Gly
- ExAC rs752089909
- gnomAD rs752089909
- Missense
- Variant Prioritization Score for Impact Estimate 0.266
- REVEL 0.22
- CADD 21.00
- PolyPhen-2 0.34
- SIFT 0.37
- Population evidence available
- Structural context available