D28V (p.Asp28Val) variant of UNC13D (Protein unc-13 homolog D)
D28V (p.Asp28Val) in UNC13D (Protein unc-13 homolog D) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
D28V (p.Asp28Val) variant details
- p.Asp28Val
- ExAC rs756041281
- gnomAD rs756041281
- Missense
- Variant Prioritization Score for Impact Estimate 0.28
- REVEL 0.22
- CADD 23.00
- PolyPhen-2 0.02
- SIFT 0.01
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available