V24G (p.Val24Gly) variant of FLCN (Folliculin)
V24G (p.Val24Gly) in FLCN (Folliculin) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
V24G (p.Val24Gly) variant details
- p.Val24Gly
- Ensembl rs2145048967
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available