G19R (p.Gly19Arg) variant of SLC37A4 (O43826)
G19R (p.Gly19Arg) in SLC37A4 (O43826) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Phosphate transport defect; Glucose-6-phosphate transport defect. The record also includes structural context.
G19R (p.Gly19Arg) variant details
- p.Gly19Arg
- ExAC rs781942514
- Uncertain significance
- Phosphate transport defect; Glucose-6-phosphate transport defect
- Missense
- ClinVar: Uncertain significance (Phosphate transport defect; Glucose-6-phosphate transport defect)
- UniProt: Uncertain significance
- Structural context available