I38M (p.Ile38Met) variant of IFNGR2 (Interferon gamma receptor 2)
I38M (p.Ile38Met) in IFNGR2 (Interferon gamma receptor 2) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
I38M (p.Ile38Met) variant details
- p.Ile38Met
- TOPMed rs1366701907
- gnomAD rs1366701907
- Missense
- Variant Prioritization Score for Impact Estimate 0.221
- REVEL 0.20
- MetaLR 0.36
- MetaSVM -0.64
- CADD 17.00
- SIFT 0.12
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available