S99F (p.Ser99Phe) variant of F11 (Coagulation factor XI)
S99F (p.Ser99Phe) in F11 (Coagulation factor XI) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S99F (p.Ser99Phe) variant details
- p.Ser99Phe
- NCI-TCGA Cosmic COSV5300
- cosmic curated COSV53007
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available