A11V (p.Ala11Val) variant of MYD88 (Q99836)
A11V (p.Ala11Val) 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.
A11V (p.Ala11Val) variant details
- p.Ala11Val
- ExAC rs777249439
- gnomAD rs777249439
- Missense
- Variant Prioritization Score for Impact Estimate 0.309
- CADD 4.16
- PolyPhen-2 0.02
- SIFT 0.16
- Most common in the Non-Finnish European population (allele frequency 5e-05)
- Structural context available