P33H (p.Pro33His) variant of PIM1 (P11309)
P33H (p.Pro33His) in PIM1 (P11309) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
P33H (p.Pro33His) variant details
- p.Pro33His
- gnomAD rs1437856130
- Missense
- Variant Prioritization Score for Impact Estimate 0.438
- REVEL 0.23
- CADD 23.90
- PolyPhen-2 0.08
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available