D46G (p.Asp46Gly) variant of MYD88 (Q99836)
D46G (p.Asp46Gly) in MYD88 (Q99836) 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.
D46G (p.Asp46Gly) variant details
- p.Asp46Gly
- gnomAD rs1374235413
- Missense
- Variant Prioritization Score for Impact Estimate 0.615
- CADD 27.40
- PolyPhen-2 0.13
- SIFT 0.02
- Most common in the 1KG:IBS population (allele frequency 0.017)
- Structural context available