A89V (p.Ala89Val) variant of CDKN1C (P49918)
A89V (p.Ala89Val) in CDKN1C (P49918) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
A89V (p.Ala89Val) variant details
- p.Ala89Val
- rs1564928743
- gnomAD 11-2884118-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.386
- CADD 15.40
- Most common in the Non-Finnish European population (allele frequency 1.9e-06)
- Structural context available
- Literature evidence available