V56F (p.Val56Phe) variant of F9 (Coagulation factor IX)
V56F (p.Val56Phe) in F9 (Coagulation factor IX) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V56F (p.Val56Phe) variant details
- p.Val56Phe
- NCI-TCGA Cosmic COSV9949
- cosmic curated COSV99496
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available