Q37K (p.Gln37Lys) variant of SLC2A1 (P11166)
Q37K (p.Gln37Lys) in SLC2A1 (P11166) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.77 / 1. The record also includes population frequency data and structural context.
Q37K (p.Gln37Lys) variant details
- p.Gln37Lys
- ExAC rs770013950
- gnomAD rs770013950
- Missense
- Variant Prioritization Score for Impact Estimate 0.774
- REVEL 0.78
- CADD 26.40
- PolyPhen-2 0.51
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available