A37V (p.Ala37Val) variant of UNC13D (Protein unc-13 homolog D)
A37V (p.Ala37Val) in UNC13D (Protein unc-13 homolog D) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
A37V (p.Ala37Val) variant details
- p.Ala37Val
- gnomAD rs1411928994
- Missense
- Variant Prioritization Score for Impact Estimate 0.124
- REVEL 0.06
- CADD 10.70
- PolyPhen-2 0.03
- SIFT 0.29
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available