N27N (p.Asn27Asn) variant of IL7R (P16871)
N27N (p.Asn27Asn) in IL7R (P16871) is a protein-truncating change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data, published literature, and structural context.
N27N (p.Asn27Asn) variant details
- p.Asn27Asn
- rs753451294
- gnomAD 5-35857058-T-C
- Splice Region
- Variant Prioritization Score for Impact Estimate 0.181
- CADD 14.20
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available