G34V (p.Gly34Val) variant of FLCN (Folliculin)
G34V (p.Gly34Val) in FLCN (Folliculin) 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.
G34V (p.Gly34Val) variant details
- p.Gly34Val
- cosmic curated COSV53262
- TOPMed rs2047310469
- 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