p.Gln37 Gly41delinsArg variant of SLC2A10 (O95528)
p.Gln37 Gly41delinsArg 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, published literature, and structural context.
p.Gln37 Gly41delinsArg variant details
- rs767211470
- gnomAD 20-46725145-CAGCT
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.546
- CADD 18.50
- Population evidence available
- Structural context available
- Literature evidence available