V39L (p.Val39Leu) variant of MYD88 (Q99836)
V39L (p.Val39Leu) in MYD88 (Q99836) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
V39L (p.Val39Leu) variant details
- p.Val39Leu
- ExAC rs770387646
- TOPMed rs770387646
- gnomAD rs770387646
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available