Q37H (p.Gln37His) variant of SLC2A1 (P11166)
Q37H (p.Gln37His) in SLC2A1 (P11166) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
Q37H (p.Gln37His) variant details
- p.Gln37His
- rs2525034775
- ClinGen CA339964733
- ClinVar RCV003227208
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available