E36G (p.Glu36Gly) variant of FLCN (Folliculin)
E36G (p.Glu36Gly) in FLCN (Folliculin) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely benign in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
E36G (p.Glu36Gly) variant details
- p.Glu36Gly
- Ensembl rs2145047161
- Likely benign
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Likely benign (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available