A3V (p.Ala3Val) variant of MYD88 (Q99836)
A3V (p.Ala3Val) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
A3V (p.Ala3Val) variant details
- p.Ala3Val
- ExAC rs779461452
- gnomAD rs779461452
- Missense
- Variant Prioritization Score for Impact Estimate 0.306
- CADD 14.00
- PolyPhen-2 0.00
- SIFT 0.24
- Most common in the Ashkenazi Jewish population (allele frequency 5.1e-05)
- Structural context available