G38S (p.Gly38Ser) variant of G6PD (P11413)
G38S (p.Gly38Ser) in G6PD (P11413) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified. The record also includes structural context.
G38S (p.Gly38Ser) variant details
- p.Gly38Ser
- rs2523308296
- ClinGen CA415201737
- ClinVar RCV003490884
- Uncertain significance
- not specified
- Missense
- ClinVar: Uncertain significance (not specified)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available