P17P (p.Pro17Pro) variant of CEBPB (P17676)
P17P (p.Pro17Pro) in CEBPB (P17676) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data, published literature, and structural context.
P17P (p.Pro17Pro) variant details
- p.Pro17Pro
- rs754328755
- gnomAD 20-50191084-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.618
- CADD 14.20
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available
- Literature evidence available