M36V (p.Met36Val) variant of UNC13D (Protein unc-13 homolog D)
M36V (p.Met36Val) in UNC13D (Protein unc-13 homolog D) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.07 / 1. The record also includes population frequency data and structural context.
M36V (p.Met36Val) variant details
- p.Met36Val
- gnomAD rs1358667977
- Missense
- Variant Prioritization Score for Impact Estimate 0.0741
- REVEL 0.05
- CADD 6.56
- PolyPhen-2 0.00
- SIFT 0.27
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available