Q36E (p.Gln36Glu) variant of SLC2A2 (P11168)
Q36E (p.Gln36Glu) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
Q36E (p.Gln36Glu) variant details
- p.Gln36Glu
- TOPMed rs1158195535
- gnomAD rs1158195535
- Missense
- Variant Prioritization Score for Impact Estimate 0.21
- REVEL 0.18
- CADD 15.90
- PolyPhen-2 0.00
- SIFT 0.28
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available