I13V (p.Ile13Val) variant of F13B (Coagulation factor XIII B chain)
I13V (p.Ile13Val) in F13B (Coagulation factor XIII B chain) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data and structural context.
I13V (p.Ile13Val) variant details
- p.Ile13Val
- NCI-TCGA Cosmic COSV1008
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.0598
- REVEL 0.04
- CADD 2.34
- PolyPhen-2 0.00
- SIFT 0.55
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available