A3D (p.Ala3Asp) variant of MET (P08581)
A3D (p.Ala3Asp) 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.
A3D (p.Ala3Asp) variant details
- p.Ala3Asp
- Ensembl rs1797064164
- 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