V18D (p.Val18Asp) variant of CD40 (P25942)
V18D (p.Val18Asp) in CD40 (P25942) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes population frequency data and structural context.
V18D (p.Val18Asp) variant details
- p.Val18Asp
- gnomAD rs2085324142
- Missense
- Variant Prioritization Score for Impact Estimate 0.615
- REVEL 0.64
- CADD 29.00
- Most common in the Latino/Admixed American population (allele frequency 6.6e-05)
- Structural context available