N79T (p.Asn79Thr) variant of IFNGR1 (Interferon gamma receptor 1)
N79T (p.Asn79Thr) in IFNGR1 (Interferon gamma receptor 1) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes population frequency data and structural context.
N79T (p.Asn79Thr) variant details
- p.Asn79Thr
- cosmic curated COSV10820
- 1000Genomes rs377227464
- ESP rs377227464
- ExAC rs377227464
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available