P15T (p.Pro15Thr) variant of CEBPB (P17676)
P15T (p.Pro15Thr) in CEBPB (P17676) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data, published literature, and structural context.
P15T (p.Pro15Thr) variant details
- p.Pro15Thr
- gnomAD 20-50191076-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.266
- REVEL 0.05
- CADD 20.50
- PolyPhen-2 0.64
- SIFT 0.28
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available
- Literature evidence available