A23T (p.Ala23Thr) variant of MYD88 (Q99836)
A23T (p.Ala23Thr) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data and structural context.
A23T (p.Ala23Thr) variant details
- p.Ala23Thr
- ExAC rs750178090
- gnomAD rs750178090
- Missense
- Variant Prioritization Score for Impact Estimate 0.457
- CADD 10.70
- PolyPhen-2 0.00
- SIFT 0.73
- Most common in the Non-Finnish European population (allele frequency 1.6e-05)
- Structural context available