N39N (p.Asn39Asn) variant of IFNG (Interferon gamma)
N39N (p.Asn39Asn) in IFNG (Interferon gamma) is a protein-truncating change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
N39N (p.Asn39Asn) variant details
- p.Asn39Asn
- rs1309260379
- gnomAD 12-68158257-A-G
- Splice Region
- Variant Prioritization Score for Impact Estimate 0.0953
- CADD 2.07
- Most common in the Non-Finnish European population (allele frequency 4.9e-05)
- Structural context available
- Literature evidence available