A6V (p.Ala6Val) variant of FLCN (Folliculin)
A6V (p.Ala6Val) 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.
A6V (p.Ala6Val) variant details
- p.Ala6Val
- NCI-TCGA TCGA novel
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available