I149M (p.Ile149Met) variant of F12 (Coagulation factor XII)
I149M (p.Ile149Met) in F12 (Coagulation factor XII) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
I149M (p.Ile149Met) variant details
- p.Ile149Met
- NCI-TCGA Cosmic COSV5369
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available