N18D (p.Asn18Asp) variant of PIM1 (P11309)
N18D (p.Asn18Asp) 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.
N18D (p.Asn18Asp) variant details
- p.Asn18Asp
- TOPMed rs1186895104
- gnomAD rs1186895104
- Missense
- Variant Prioritization Score for Impact Estimate 0.155
- REVEL 0.04
- CADD 15.00
- PolyPhen-2 0.04
- SIFT 0.64
- Most common in the African/African-American population (allele frequency 0.00012)
- Structural context available