V37L (p.Val37Leu) variant of DDX41 (Q9UJV9)
V37L (p.Val37Leu) 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.
V37L (p.Val37Leu) variant details
- p.Val37Leu
- cosmic curated COSV10881
- Ensembl rs2127438052
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available