Q39H (p.Gln39His) variant of PIM1 (P11309)
Q39H (p.Gln39His) in PIM1 (P11309) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
Q39H (p.Gln39His) variant details
- p.Gln39His
- ExAC rs767621897
- TOPMed rs767621897
- gnomAD rs767621897
- Missense
- Variant Prioritization Score for Impact Estimate 0.31
- REVEL 0.09
- CADD 22.80
- PolyPhen-2 0.05
- SIFT 0.21
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available