R28Q (p.Arg28Gln) variant of MYD88 (Q99836)
R28Q (p.Arg28Gln) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data and structural context.
R28Q (p.Arg28Gln) variant details
- p.Arg28Gln
- Ensembl rs1700991485
- Missense
- Variant Prioritization Score for Impact Estimate 0.561
- CADD 23.90
- PolyPhen-2 0.02
- SIFT 0.47
- Most common in the 1KG:IBS population (allele frequency 0.017)
- Structural context available