N49N (p.Asn49Asn) variant of IL7R (P16871)
N49N (p.Asn49Asn) in IL7R (P16871) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data, published literature, and structural context.
N49N (p.Asn49Asn) variant details
- p.Asn49Asn
- gnomAD 5-35860916-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.134
- CADD 7.57
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available