| ALK gene rearrangement |
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| Antithrombin Deficiency screen for detection of familial mutation (SERPINC1) |
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| BCR-ABL1 t(9;22)(q34;q11) Diagnostic (for suspected CML) |
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| BCR-ABL1 t(9;22)(q34;q11) E1A2, E13A2 & E14A2 transcripts Diagnostic Acute Leukaemia |
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| BRAF mutation analysis |
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| CBFB-MYH11 inv(16) / t(16;16) Diagnostic (AML) |
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| DPYD Genotyping |
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| EGFR mutation analysis (blood) |
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| EGFR mutation analysis (FFPE) |
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| ETV6-RUNX1 t(12;21)(p13;q22) Diagnostic (ALL) |
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| FIP1L1-PDGFRA fusion gene |
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| FLT3 |
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| FOXL2 mutation analysis |
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| Haemophilia A full genetic screen |
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| HER2 gene amplification |
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| IDH1 and IDH2 mutation analysis |
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| Immunoglobulin HV Gene Sequencing |
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| KIT and PDGFRA mutation analysis |
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| KIT D816V Mutation Testing |
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| KMT2A (MLL, 11q23) rearrangement Diagnostic test for Acute Leukaemia |
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| KRAS mutation analysis |
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| MGMT promoter methylation analysis |
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| Mismatch repair testing |
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| MRD monitoring for BCR-ABL1 E13A2 and/or E14A2 transcripts |
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| MRD monitoring for BCR-ABL1 E1A2 transcript |
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| Next Generation Sequencing (NGS) for Myeloid Disorders |
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| NPM1 |
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| NRAS mutation analysis |
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| PD-L1 immunohistochemistry |
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| PML-RARA t(15;17)(q22;q21) Diagnostic (AML) |
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| ROS1 gene rearrangement |
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| RUNX1-RUNX1T1 t(8:21)(q22;q22) Diagnostic (AML) |
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| TCF3-PBX1 t(1;19)(q23;p13) Diagnostic (ALL) |
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| TCR Gene Clonality |
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| TP53 |
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