N8N (p.Asn8Asn) variant of CDKN1B (P46527)
N8N (p.Asn8Asn) in CDKN1B (P46527) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data, published literature, and structural context.
N8N (p.Asn8Asn) variant details
- p.Asn8Asn
- rs371308246
- gnomAD 12-12717863-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.459
- CADD 13.70
- Most common in the African/African-American population (allele frequency 0.00024)
- Structural context available
- Literature evidence available