S13F (p.Ser13Phe) variant of F10 (Coagulation factor X)
S13F (p.Ser13Phe) in F10 (Coagulation factor X) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S13F (p.Ser13Phe) variant details
- p.Ser13Phe
- NCI-TCGA Cosmic COSV6064
- cosmic curated COSV60645
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available