E68D (p.Glu68Asp) variant of F11 (Coagulation factor XI)
E68D (p.Glu68Asp) 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.
E68D (p.Glu68Asp) variant details
- p.Glu68Asp
- NCI-TCGA Cosmic COSV9925
- cosmic curated COSV99251
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available