G139R (p.Gly139Arg) variant of F13B (Coagulation factor XIII B chain)
G139R (p.Gly139Arg) in F13B (Coagulation factor XIII B chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.77 / 1. The record also includes population frequency data and structural context.
G139R (p.Gly139Arg) variant details
- p.Gly139Arg
- 1000Genomes rs368129885
- ESP rs368129885
- ExAC rs368129885
- TOPMed rs368129885
- Missense
- Variant Prioritization Score for Impact Estimate 0.769
- REVEL 0.75
- CADD 27.00
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the HGDP:MANDENKA population (allele frequency 0.05)
- Structural context available