P33L (p.Pro33Leu) variant of PIM1 (P11309)
P33L (p.Pro33Leu) in PIM1 (P11309) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data, published literature, and structural context.
P33L (p.Pro33Leu) variant details
- p.Pro33Leu
- gnomAD 6-37170788-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.464
- REVEL 0.28
- CADD 24.30
- PolyPhen-2 0.19
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available