R28G (p.Arg28Gly) variant of MYD88 (Q99836)
R28G (p.Arg28Gly) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
R28G (p.Arg28Gly) variant details
- p.Arg28Gly
- ExAC rs779805093
- TOPMed rs779805093
- gnomAD rs779805093
- Missense
- Variant Prioritization Score for Impact Estimate 0.445
- CADD 21.30
- PolyPhen-2 0.00
- SIFT 0.35
- Most common in the Finnish in Finland (FIN) population (allele frequency 3.8e-05)
- Structural context available