N38N (p.Asn38Asn) variant of F9 (Coagulation factor IX)
N38N (p.Asn38Asn) in F9 (Coagulation factor IX) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data, published literature, and structural context.
N38N (p.Asn38Asn) variant details
- p.Asn38Asn
- rs745353370
- gnomAD X-139537035-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.214
- CADD 7.26
- Most common in the 1KG:STU population (allele frequency 0.0073)
- Structural context available
- Literature evidence available