D17D (p.Asp17Asp) variant of CDKN1B (P46527)
D17D (p.Asp17Asp) 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.
D17D (p.Asp17Asp) variant details
- p.Asp17Asp
- rs552533838
- gnomAD 12-12717890-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.46
- CADD 13.80
- Most common in the 1KG:ITU population (allele frequency 0.0049)
- Structural context available
- Literature evidence available