Q37H (p.Gln37His) variant of SLC2A10 (O95528)
Q37H (p.Gln37His) in SLC2A10 (O95528) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data, published literature, and structural context.
Q37H (p.Gln37His) variant details
- p.Gln37His
- gnomAD 20-46709999-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.175
- CADD 2.27
- Population evidence available
- Structural context available
- Literature evidence available