P32H (p.Pro32His) variant of UNC13D (Protein unc-13 homolog D)
P32H (p.Pro32His) 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.
P32H (p.Pro32His) variant details
- p.Pro32His
- ExAC rs766863447
- TOPMed rs766863447
- gnomAD rs766863447
- Missense
- Variant Prioritization Score for Impact Estimate 0.279
- REVEL 0.14
- CADD 23.60
- PolyPhen-2 0.50
- SIFT 0.01
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available