N9D (p.Asn9Asp) variant of FGG (Fibrinogen gamma chain)
N9D (p.Asn9Asp) in FGG (Fibrinogen gamma chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
N9D (p.Asn9Asp) variant details
- p.Asn9Asp
- Ensembl rs1731241392
- Missense
- Variant Prioritization Score for Impact Estimate 0.0857
- REVEL 0.02
- CADD 10.50
- PolyPhen-2 0.01
- SIFT 0.26
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available