T14A (p.Thr14Ala) variant of F11 (Coagulation factor XI)
T14A (p.Thr14Ala) in F11 (Coagulation factor XI) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
T14A (p.Thr14Ala) variant details
- p.Thr14Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available