G127R (p.Gly127Arg) variant of F13B (Coagulation factor XIII B chain)
G127R (p.Gly127Arg) in F13B (Coagulation factor XIII B chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data and structural context.
G127R (p.Gly127Arg) variant details
- p.Gly127Arg
- TOPMed rs1558312007
- Missense
- Variant Prioritization Score for Impact Estimate 0.58
- REVEL 0.44
- CADD 25.20
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available