G17E (p.Gly17Glu) variant of BARD1 (Q99728)
G17E (p.Gly17Glu) in BARD1 (Q99728) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
G17E (p.Gly17Glu) variant details
- p.Gly17Glu
- Ensembl rs1574869785
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available