V43L (p.Val43Leu) variant of MYD88 (Q99836)
V43L (p.Val43Leu) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data and structural context.
V43L (p.Val43Leu) variant details
- p.Val43Leu
- ExAC rs774701316
- gnomAD rs774701316
- Missense
- Variant Prioritization Score for Impact Estimate 0.55
- CADD 23.10
- PolyPhen-2 0.02
- SIFT 0.14
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available