D46N (p.Asp46Asn) variant of MYD88 (Q99836)
D46N (p.Asp46Asn) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.74 / 1. The record also includes population frequency data and structural context.
D46N (p.Asp46Asn) variant details
- p.Asp46Asn
- gnomAD rs980606265
- Missense
- Variant Prioritization Score for Impact Estimate 0.743
- CADD 25.00
- PolyPhen-2 0.44
- SIFT 0.08
- Most common in the Middle Eastern population (allele frequency 0.0011)
- Structural context available