N39D (p.Asn39Asp) variant of IFNG (Interferon gamma)
N39D (p.Asn39Asp) in IFNG (Interferon gamma) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data, published literature, and structural context.
N39D (p.Asn39Asp) variant details
- p.Asn39Asp
- gnomAD 12-68158259-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.298
- REVEL 0.21
- MetaLR 0.16
- MetaSVM -0.90
- CADD 21.00
- PolyPhen-2 0.10
- SIFT 0.02
- Most common in the South Asian population (allele frequency 1.3e-05)
- Structural context available
- Literature evidence available