W140* (p.Trp140Ter) variant of F13B (Coagulation factor XIII B chain)
W140* (p.Trp140Ter) in F13B (Coagulation factor XIII B chain) is a protein-truncating change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.86 / 1. The record also includes population frequency data and structural context.
W140* (p.Trp140Ter) variant details
- p.Trp140Ter
- NCI-TCGA Cosmic COSV1008
- Variant assessed as somatic; high impact.
- Stop Gained
- Variant Prioritization Score for Impact Estimate 0.856
- CADD 37.00
- UniProt: Variant assessed as somatic; high impact.
- Most common in the Non-Finnish European population (allele frequency 4.5e-06)
- Structural context available