G33R (p.Gly33Arg) variant of F13B (Coagulation factor XIII B chain)
G33R (p.Gly33Arg) in F13B (Coagulation factor XIII B chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.67 / 1. The record also includes population frequency data and structural context.
G33R (p.Gly33Arg) variant details
- p.Gly33Arg
- gnomAD rs1184878385
- Missense
- Variant Prioritization Score for Impact Estimate 0.667
- REVEL 0.57
- CADD 26.70
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available