Y4N (p.Tyr4Asn) variant of IL2RA (P01589)
Y4N (p.Tyr4Asn) in IL2RA (P01589) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The available variant effect predictions contribute to a CATVariant prioritization score of 0.04 / 1. The record also includes population frequency data and structural context.
Y4N (p.Tyr4Asn) variant details
- p.Tyr4Asn
- gnomAD rs1564556393
- Uncertain significance
- Missense
- Variant Prioritization Score for Impact Estimate 0.0417
- REVEL 0.01
- CADD 0.01
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available