H93Q (p.His93Gln) variant of DDX41 (Q9UJV9)
H93Q (p.His93Gln) in DDX41 (Q9UJV9) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes structural context.
H93Q (p.His93Gln) variant details
- p.His93Gln
- TOPMed rs1340906536
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available