L29V (p.Leu29Val) variant of UNC13D (Protein unc-13 homolog D)
L29V (p.Leu29Val) in UNC13D (Protein unc-13 homolog D) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
L29V (p.Leu29Val) variant details
- p.Leu29Val
- gnomAD rs2064970609
- Missense
- Variant Prioritization Score for Impact Estimate 0.135
- REVEL 0.07
- CADD 11.10
- PolyPhen-2 0.01
- SIFT 0.36
- Most common in the East Asian population (allele frequency 0.00015)
- Structural context available