N23S (p.Asn23Ser) variant of MET (P08581)
N23S (p.Asn23Ser) in MET (P08581) 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.
N23S (p.Asn23Ser) variant details
- p.Asn23Ser
- Ensembl rs2116579413
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available