| # | Rank | Epic Display Name | Cerner Name | SCM Name | AEHR Name | Cerner PDM | EPIC Procedure Master Number | Informatics Workgroup | 
                    
                | 1. | 99999 | B Cell Gene Rearrangement (IGR) Molecular Detection | HLX IGR by PCR Case | Molecular Genetics - IGR |  | 5160170 | LAB11400 | Molpath inhouse | 
                    
                | 2. | 99999 | Calreticulin (CALR) Mutation Molecular Detection | HLX CALR CASE | Calreticulin Gene Mutation Analysis | HLX Calreticulin Case (HLX CALR CASE) | 1763033 | LAB11646 | Molpath inhouse | 
                    
                | 3. | 99999 | CXCR4 C1013G Mutation Molecular Detection |  |  |  | 248466 | LAB14273 | Molpath Inhouse | 
                    
                | 4. | 99999 | Factor 5 Leiden Mutation Molecular Detection | HLX Factor V Leiden CASE | Molecular Genetics - Factor V Leiden | Factor V Leiden | 5160174 | LAB346 | Molpath inhouse | 
                    
                | 5. | 99999 | FLT3 ITD-TKD Mutation Molecular Detection | HLX FLT3 CASE | FLT3 ITD MUTATION ANALYSIS | FLT3-ITD Mutation Analysis | 1863168 | LAB11399 | Molpath inhouse | 
                    
                | 6. | 99999 | Fragile X Mutation (FMR1) Molecular Detection | HLX Fragile X CASE | Fragile X CASE | Fragile X DNA Probe | 5160403 | LAB11647 | Molpath inhouse | 
                    
                | 7. | 99999 | Hemochromatosis (HFE) Mutation Molecular Detection | HLX HEMOCHROMATOSIS CASE | Hemochromatosis Gene Mutation | Hemochromatosis Gene Mutation | 5160990 | LAB833 | Molpath inhouse | 
                    
                | 8. | 99999 | Hereditary Inclusion Body Myopathy (HIBM) Mutation Molecular Detection | HLX HIBM CASE |  | HIBM | 5157200 | LAB11454 | Molpath inhouse | 
                    
                | 9. | 99999 | HLA B27 Molecular Detection | HLX HLA B27 Genotype Case | HLA B27 Genotyping | HLA B27 Genotyping | 238466 | LAB11402 | Molpath inhouse | 
                    
                | 10. | 99999 | HLA B57:01 Molecular Detection | HLX HLA Antigen B5701 Case | HLX HLA B57-01 Antigen Case | HLX HLA B57-01 Antigen Case | 228468 | LAB11403 | Molpath inhouse | 
                    
                | 11. | 99999 | JAK2 Exons 12-15 Mutation Analysis |  |  |  | 248470 | LAB4151 | Molpath Inhouse | 
                    
                | 12. | 99999 | MPL Mutation Molecular Detection | HLX MPL Mutation Analysis Case | MPL Mutation Analysis | MPL Mutation Analysis Case | 1559701 | LAB11404 | Molpath inhouse | 
                    
                | 13. | 99999 | MTHFR Mutation Molecular Detection | HLX MTHFR CASE | Molecular Genetics - MTHFR Gene Case | HLX MTHFR Case | 5160200 | LAB11455 | Molpath inhouse | 
                    
                | 14. | 99999 | MYD88 and CXCR4 Panel Molecular Detection |  |  |  | 248468 | LAB14270 | Molpath Inhouse | 
                    
                | 15. | 99999 | MYD88 L265P Mutation Molecular Detection |  |  |  | 248467 | LAB14271 | Molpath Inhouse | 
                    
                | 16. | 99999 | Prothrombin (PTR) Mutation Molecular Detection | HLX Prothrombin CASE | Molecular Genetics - Prothrombin | Prothrombin Gene Mutation | 5160177 | LAB834 | Molpath inhouse | 
                    
                | 17. | 99999 | Quantitative BCR/ABL Molecular Detection | HLX BCR-ABL by RT-PCR CASE | BCR/ABL By RT - PCR Quantitative | BCR/ABL Quantitative | 5911120 | LAB11398 | Molpath inhouse | 
                    
                | 18. | 99999 | Quantitative JAK2 V617F Mutation Molecular Detection | HLX JAK-2 Mutation CASE | JAK2 Mutation | Molecular JAK2 Assay | 5160105 | LAB11401 | Molpath inhouse | 
                    
                | 19. | 99999 | Spinal Muscular Atrophy (SMA) Molecular Detection | HLX Spinal Muscular Atrophy (SMA) Case | Spinal Muscular Atrophy | Spinal Muscular Atrophy | 5910160 | LAB11648 | Molpath inhouse | 
                    
                | 20. | 99999 | T Cell Gene Rearrangement (TCR) Molecular Detection | HLX TCR by PCR Case | Molecular Genetics - TCR |  | 5160176 | LAB11405 | Molpath Inhouse | 
                    
                | 21. | 99999 | Y Chromosome Microdeletion Mutation Molecular Detection |  |  |  | 248471 | LAB14269 | Molpath Inhouse |