L18F (p.Leu18Phe) variant of MET (P08581)
L18F (p.Leu18Phe) in MET (P08581) 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.
L18F (p.Leu18Phe) variant details
- p.Leu18Phe
- cosmic curated COSV59266
- Ensembl rs2116579018
- 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