G40D (p.Gly40Asp) variant of CD79B (P40259)
G40D (p.Gly40Asp) in CD79B (P40259) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.60 / 1. The record also includes population frequency data and structural context.
G40D (p.Gly40Asp) variant details
- p.Gly40Asp
- TOPMed rs1908053862
- gnomAD rs1908053862
- Missense
- Variant Prioritization Score for Impact Estimate 0.597
- REVEL 0.64
- CADD 23.60
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available