Q37K (p.Gln37Lys) variant of PIM1 (P11309)
Q37K (p.Gln37Lys) 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.
Q37K (p.Gln37Lys) variant details
- p.Gln37Lys
- 1000Genomes rs2113769440
- Missense
- Variant Prioritization Score for Impact Estimate 0.329
- REVEL 0.07
- CADD 18.80
- Most common in the 1KG:CHS population (allele frequency 0.0049)
- Structural context available