N3N (p.Asn3Asn) variant of CDKN1B (P46527)
N3N (p.Asn3Asn) in CDKN1B (P46527) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data, published literature, and structural context.
N3N (p.Asn3Asn) variant details
- p.Asn3Asn
- rs1411622351
- gnomAD 12-12717848-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.453
- CADD 13.60
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available
- Literature evidence available