F88L (p.Phe88Leu) variant of F13B (Coagulation factor XIII B chain)
F88L (p.Phe88Leu) in F13B (Coagulation factor XIII B chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
F88L (p.Phe88Leu) variant details
- p.Phe88Leu
- gnomAD rs1356843456
- Missense
- Variant Prioritization Score for Impact Estimate 0.226
- REVEL 0.11
- CADD 20.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available