G9G (p.Gly9Gly) variant of CDKN1B (P46527)
G9G (p.Gly9Gly) in CDKN1B (P46527) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data, published literature, and structural context.
G9G (p.Gly9Gly) variant details
- p.Gly9Gly
- rs1060503869
- gnomAD 12-12717866-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.506
- CADD 14.40
- Most common in the Non-Finnish European population (allele frequency 6.3e-06)
- Structural context available
- Literature evidence available