L13F (p.Leu13Phe) variant of FLCN (Folliculin)
L13F (p.Leu13Phe) 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.
L13F (p.Leu13Phe) variant details
- p.Leu13Phe
- Ensembl rs2145050302
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available