V13G (p.Val13Gly) variant of MET (P08581)
V13G (p.Val13Gly) in MET (P08581) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
V13G (p.Val13Gly) variant details
- p.Val13Gly
- ExAC rs748776466
- TOPMed rs748776466
- gnomAD rs748776466
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available