G38A (p.Gly38Ala) variant of KCNQ2 (O43526)
G38A (p.Gly38Ala) in KCNQ2 (O43526) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Early-infantile DEE. The record also includes structural context.
G38A (p.Gly38Ala) variant details
- p.Gly38Ala
- rs2516745799
- ClinGen CA409635665
- ClinVar RCV006563140
- Uncertain significance
- Early-infantile DEE
- Missense
- ClinVar: Uncertain significance (Early-infantile DEE)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available