N18H (p.Asn18His) variant of PIM1 (P11309)
N18H (p.Asn18His) in PIM1 (P11309) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and structural context.
N18H (p.Asn18His) variant details
- p.Asn18His
- TOPMed rs1186895104
- gnomAD rs1186895104
- Missense
- Variant Prioritization Score for Impact Estimate 0.157
- REVEL 0.05
- CADD 16.20
- PolyPhen-2 0.01
- SIFT 0.12
- Population evidence available
- Structural context available