Q51H (p.Gln51His) variant of UNC13D (Protein unc-13 homolog D)
Q51H (p.Gln51His) in UNC13D (Protein unc-13 homolog D) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
Q51H (p.Gln51His) variant details
- p.Gln51His
- ESP rs139726111
- ExAC rs139726111
- TOPMed rs139726111
- gnomAD rs139726111
- Missense
- Variant Prioritization Score for Impact Estimate 0.399
- REVEL 0.09
- CADD 33.00
- PolyPhen-2 0.26
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available