C17F (p.Cys17Phe) variant of PIM1 (P11309)
C17F (p.Cys17Phe) in PIM1 (P11309) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
C17F (p.Cys17Phe) variant details
- p.Cys17Phe
- 1000Genomes rs532972131
- TOPMed rs532972131
- gnomAD rs532972131
- Missense
- Variant Prioritization Score for Impact Estimate 0.332
- REVEL 0.06
- CADD 21.90
- PolyPhen-2 0.00
- SIFT 0.33
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available