P19del (p.Pro19del) variant of CEBPB (P17676)
P19del (p.Pro19del) in CEBPB (P17676) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data, published literature, and structural context.
P19del (p.Pro19del) variant details
- rs760594355
- gnomAD 20-50191074-TGCC-
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.411
- CADD 15.30
- Most common in the African/African-American population (allele frequency 0.00031)
- Structural context available
- Literature evidence available