A51V (p.Ala51Val) variant of MYD88 (Q99836)
A51V (p.Ala51Val) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.69 / 1. The record also includes population frequency data and structural context.
A51V (p.Ala51Val) variant details
- p.Ala51Val
- ExAC rs761769496
- Missense
- Variant Prioritization Score for Impact Estimate 0.688
- CADD 27.90
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the Ashkenazi Jewish population (allele frequency 5.1e-05)
- Structural context available