M27L (p.Met27Leu) variant of MYD88 (Q99836)
M27L (p.Met27Leu) in MYD88 (Q99836) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Pyogenic bacterial infections due to MyD88 deficiency. The record also includes structural context.
M27L (p.Met27Leu) variant details
- p.Met27Leu
- TOPMed rs1700991048
- Uncertain significance
- Pyogenic bacterial infections due to MyD88 deficiency
- Missense
- ClinVar: Uncertain significance (Pyogenic bacterial infections due to MyD88 deficiency)
- UniProt: Uncertain significance
- Structural context available