R19R (p.Arg19Arg) variant of CDKN1B (P46527)
R19R (p.Arg19Arg) in CDKN1B (P46527) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
R19R (p.Arg19Arg) variant details
- p.Arg19Arg
- rs1946487176
- gnomAD 12-12717896-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.15
- CADD 9.81
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available