W47* (p.Trp47Ter) variant of MYD88 (Q99836)
W47* (p.Trp47Ter) in MYD88 (Q99836) is a protein-truncating change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.68 / 1. The record also includes population frequency data and structural context.
W47* (p.Trp47Ter) variant details
- p.Trp47Ter
- Ensembl rs2125775607
- Stop Gained
- Variant Prioritization Score for Impact Estimate 0.681
- CADD 32.00
- Most common in the Non-Finnish European population (allele frequency 2.3e-05)
- Structural context available