G148V (p.Gly148Val) variant of UNC13D (Protein unc-13 homolog D)
G148V (p.Gly148Val) in UNC13D (Protein unc-13 homolog D) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
G148V (p.Gly148Val) variant details
- p.Gly148Val
- 1000Genomes rs551855408
- ExAC rs551855408
- TOPMed rs551855408
- gnomAD rs551855408
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available