S86N (p.Ser86Asn) variant of CDKN1C (P49918)
S86N (p.Ser86Asn) in CDKN1C (P49918) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data, published literature, and structural context.
S86N (p.Ser86Asn) variant details
- p.Ser86Asn
- rs1314520245
- gnomAD 11-2884097-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.238
- CADD 9.40
- Most common in the East Asian population (allele frequency 0.00011)
- Structural context available
- Literature evidence available