N78D (p.Asn78Asp) variant of FGA (Fibrinogen alpha chain)
N78D (p.Asn78Asp) in FGA (Fibrinogen alpha chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data.
N78D (p.Asn78Asp) variant details
- p.Asn78Asp
- gnomAD rs1485772303
- Missense
- Variant Prioritization Score for Impact Estimate 0.279
- REVEL 0.24
- CADD 18.40
- PolyPhen-2 0.04
- SIFT 0.31
- Most common in the Non-Finnish European population (allele frequency 9e-07)