E29G (p.Glu29Gly) variant of SCN4A (Nav1.4)
E29G (p.Glu29Gly) in SCN4A (Nav1.4) 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.
E29G (p.Glu29Gly) variant details
- p.Glu29Gly
- rs144347844
- ClinGen CA292972909
- ClinVar RCV002509925
- 1000Genomes rs144347844
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available