R129G (p.Arg129Gly) variant of FGA (Fibrinogen alpha chain)
R129G (p.Arg129Gly) in FGA (Fibrinogen alpha chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data.
R129G (p.Arg129Gly) variant details
- p.Arg129Gly
- ExAC rs781289913
- TOPMed rs781289913
- gnomAD rs781289913
- Missense
- Variant Prioritization Score for Impact Estimate 0.496
- REVEL 0.40
- CADD 23.20
- PolyPhen-2 0.11
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 3.6e-06)