R77S (p.Arg77Ser) variant of SLC37A4 (O43826)
R77S (p.Arg77Ser) in SLC37A4 (O43826) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Glucose-6-phosphate transport defect. The available variant effect predictions contribute to a CATVariant prioritization score of 0.78 / 1. The record also includes population frequency data and structural context.
R77S (p.Arg77Ser) variant details
- p.Arg77Ser
- TOPMed rs1417623185
- gnomAD rs1417623185
- Uncertain significance
- Glucose-6-phosphate transport defect
- Missense
- Variant Prioritization Score for Impact Estimate 0.783
- CADD 26.20
- PolyPhen-2 1.00
- SIFT 0.04
- ClinVar: Uncertain significance (Glucose-6-phosphate transport defect)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available