L35P (p.Leu35Pro) variant of F10 (Coagulation factor X)
L35P (p.Leu35Pro) in F10 (Coagulation factor X) 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.
L35P (p.Leu35Pro) variant details
- p.Leu35Pro
- Ensembl rs920680221
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available