P6L (p.Pro6Leu) variant of MYD88 (Q99836)
P6L (p.Pro6Leu) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
P6L (p.Pro6Leu) variant details
- p.Pro6Leu
- Ensembl rs1700986467
- Missense
- Variant Prioritization Score for Impact Estimate 0.265
- CADD 17.30
- Most common in the Non-Finnish European population (allele frequency 5.8e-05)
- Structural context available