I9F (p.Ile9Phe) variant of F13B (Coagulation factor XIII B chain)
I9F (p.Ile9Phe) in F13B (Coagulation factor XIII B chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data and structural context.
I9F (p.Ile9Phe) variant details
- p.Ile9Phe
- TOPMed rs1656090778
- gnomAD rs1656090778
- Missense
- Variant Prioritization Score for Impact Estimate 0.111
- REVEL 0.06
- CADD 13.30
- PolyPhen-2 0.00
- SIFT 0.90
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available