H129R (p.His129Arg) variant of FGG (Fibrinogen gamma chain)
H129R (p.His129Arg) in FGG (Fibrinogen gamma chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data and structural context.
H129R (p.His129Arg) variant details
- p.His129Arg
- gnomAD rs1197720383
- Missense
- Variant Prioritization Score for Impact Estimate 0.513
- REVEL 0.44
- CADD 23.90
- PolyPhen-2 0.49
- SIFT 0.03
- Most common in the REMAINING population (allele frequency 3.3e-05)
- Structural context available