P26P (p.Pro26Pro) variant of CDKN1B (P46527)
P26P (p.Pro26Pro) in CDKN1B (P46527) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.49 / 1. The record also includes population frequency data, published literature, and structural context.
P26P (p.Pro26Pro) variant details
- p.Pro26Pro
- rs761630889
- gnomAD 12-12717917-C-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.494
- CADD 12.20
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available