M7I (p.Met7Ile) variant of IL2RA (P01589)
M7I (p.Met7Ile) in IL2RA (P01589) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Immunodeficiency due to CD25 deficiency. The available variant effect predictions contribute to a CATVariant prioritization score of 0.03 / 1. The record also includes population frequency data and structural context.
M7I (p.Met7Ile) variant details
- p.Met7Ile
- rs1299907703
- ClinGen CA375940497
- ClinVar RCV002038027
- TOPMed rs1299907703
- Uncertain significance
- Immunodeficiency due to CD25 deficiency
- Missense
- Variant Prioritization Score for Impact Estimate 0.0338
- REVEL 0.02
- CADD 0.15
- PolyPhen-2 0.01
- SIFT 0.26
- ClinVar: Uncertain significance (Immunodeficiency due to CD25 deficiency)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available