A44G (p.Ala44Gly) variant of MYD88 (Q99836)
A44G (p.Ala44Gly) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.73 / 1. The record also includes population frequency data and structural context.
A44G (p.Ala44Gly) variant details
- p.Ala44Gly
- TOPMed rs1426646083
- Missense
- Variant Prioritization Score for Impact Estimate 0.734
- CADD 24.80
- PolyPhen-2 0.08
- SIFT 0.21
- Most common in the African/African-American population (allele frequency 2.8e-05)
- Structural context available