V58I (p.Val58Ile) variant of PIM1 (P11309)
V58I (p.Val58Ile) in PIM1 (P11309) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
V58I (p.Val58Ile) variant details
- p.Val58Ile
- TOPMed rs896496531
- gnomAD rs896496531
- Missense
- Variant Prioritization Score for Impact Estimate 0.349
- REVEL 0.11
- CADD 18.40
- PolyPhen-2 0.00
- SIFT 0.92
- Most common in the Non-Finnish European population (allele frequency 2.8e-05)
- Structural context available