E66G (p.Glu66Gly) variant of ERCC2 (P18074)
E66G (p.Glu66Gly) in ERCC2 (P18074) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
E66G (p.Glu66Gly) variant details
- p.Glu66Gly
- TOPMed rs961564676
- gnomAD rs961564676
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available