Q37E (p.Gln37Glu) variant of SLC2A1 (P11166)
Q37E (p.Gln37Glu) in SLC2A1 (P11166) 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 and structural context.
Q37E (p.Gln37Glu) variant details
- p.Gln37Glu
- ExAC rs770013950
- gnomAD rs770013950
- Missense
- Variant Prioritization Score for Impact Estimate 0.546
- REVEL 0.42
- CADD 21.70
- PolyPhen-2 0.01
- SIFT 0.59
- Most common in the South Asian population (allele frequency 3.5e-05)
- Structural context available