S17P (p.Ser17Pro) variant of F11 (Coagulation factor XI)
S17P (p.Ser17Pro) 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.
S17P (p.Ser17Pro) variant details
- p.Ser17Pro
- NCI-TCGA Cosmic COSV9925
- cosmic curated COSV99251
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available