T17N (p.Thr17Asn) variant of MET (P08581)
T17N (p.Thr17Asn) in MET (P08581) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
T17N (p.Thr17Asn) variant details
- p.Thr17Asn
- ExAC rs747777018
- gnomAD rs747777018
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available