N27M (p.Asn27Met) variant of IL7R (P16871)
N27M (p.Asn27Met) in IL7R (P16871) is a protein-truncating change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.68 / 1. The record also includes population frequency data, published literature, and structural context.
N27M (p.Asn27Met) variant details
- p.Asn27Met
- gnomAD 5-35857053-CA-C
- Frameshift
- Variant Prioritization Score for Impact Estimate 0.676
- CADD 26.00
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available