N39T (p.Asn39Thr) variant of IFNG (Interferon gamma)
N39T (p.Asn39Thr) in IFNG (Interferon gamma) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
N39T (p.Asn39Thr) variant details
- p.Asn39Thr
- gnomAD 12-68158258-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.386
- REVEL 0.32
- MetaLR 0.26
- MetaSVM -0.55
- CADD 23.20
- PolyPhen-2 0.79
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available
- Literature evidence available