Q12H (p.Gln12His) variant of IFNGR1 (Interferon gamma receptor 1)
Q12H (p.Gln12His) in IFNGR1 (Interferon gamma receptor 1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data and structural context.
Q12H (p.Gln12His) variant details
- p.Gln12His
- NCI-TCGA Cosmic COSV1008
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.0966
- CADD 2.53
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available