Q39R (p.Gln39Arg) variant of PIM1 (P11309)
Q39R (p.Gln39Arg) in PIM1 (P11309) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
Q39R (p.Gln39Arg) variant details
- p.Gln39Arg
- TOPMed rs1387437361
- gnomAD rs1387437361
- Missense
- Variant Prioritization Score for Impact Estimate 0.285
- REVEL 0.08
- CADD 21.40
- PolyPhen-2 0.02
- SIFT 1.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available