Q39L (p.Gln39Leu) variant of PIM1 (P11309)
Q39L (p.Gln39Leu) in PIM1 (P11309) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
Q39L (p.Gln39Leu) variant details
- p.Gln39Leu
- TOPMed rs1387437361
- gnomAD rs1387437361
- Missense
- Variant Prioritization Score for Impact Estimate 0.317
- REVEL 0.12
- CADD 23.40
- PolyPhen-2 0.08
- SIFT 0.07
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available