Q37R (p.Gln37Arg) variant of SLC2A10 (O95528)
Q37R (p.Gln37Arg) in SLC2A10 (O95528) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, published literature, and structural context.
Q37R (p.Gln37Arg) variant details
- p.Gln37Arg
- gnomAD 20-46709998-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.11
- CADD 4.12
- Population evidence available
- Structural context available
- Literature evidence available