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UIDL Test Directory

Molecular Oncology Requisition

• BRAF Gene Analysis V600E with Interpretation (Exons 11, 15)
• Cancer Mutation and RNA Fusion Profile and Interpretation
• Comprehensive Lung Panel
• EGFR Gene Analysis with Interpretation (Exons 18-21)
• FGFR3 Mutation Analysis with Interpretation
• IGH Gene Clonality by PCR with Interpretation
• KIT (GIST) Targeted Gene Analysis with Interpretation (Exons 9, 11, 13, 17)
• Lung NSCLC Targeted RNA Fusions with Interpretation*
• Microsatellite Instability PCR with Interpretation
• NRAS Mutation Analysis with Interpretation (Exons 2-4)
• NTRK1,2,&3 Fusion
• PDGFRA Targeted Gene Analysis with Interpretation (Exons 12, 14, 15, 18)
• Salivary Gland Tumor Fusion Panel
• Sarcoma Fusion Panel with Interpretation*
• Thyroid Cancer Targeted RNA Fusions with Interpretation*
• TP53 Gene Analysis
• TRG Gene Clonality by PCR with Interpretation
• Tumor Gene RNA Fusion with Interpretation

Comprehensive Hematopathology Requisition

• ABL1 TKI Resistance Mutation Detection with Interpretation, Blood and Bone Marrow
• AML Mutation Profiling and Interpretation, Bone Marrow Aspirate*
• AML Mutation Profiling and Interpretation, Peripheral Blood*
• BCR/ABL1 (T(9;22)) RNA Quantitative with Interpretation, Blood
• BCR/ABL1 (T(9;22)) RNA Quantitative with Interpretation, Bone Marrow
• Calreticulin Mutation Analysis with Interpretation, Bone Marrow Aspirate
• Calreticulin Mutation Analysis with Interpretation, Whole Blood
• CEBPA Full Gene Sequence with Interpretation, Blood
• CEBPA Full Gene Sequence with Interpretation, Bone Marrow
• FLT3/NPM1 Gene Analysis with Interpretation, Blood
• FLT3/NPM1 Mutation Analysis with Interpretation, Bone Marrow
• IGH Gene Clonality by PCR with Interpretation, Tissue and Blood
• JAK2 Common Mutation V617F Analysis with Interpretation, Bone Marrow Aspirate
• JAK2 Common Mutation V617F Analysis with Interpretation, Whole Blood
• JAK2 Exon 12 Mutation, Blood
• JAK2 Exon 12 Mutation, Bone Marrow Aspirate
• JAK2 Reflex for Essential Thrombocythemia, Whole Blood*
• JAK2 Reflex for Essential Thrombocythemia, Bone Marrow Aspirate*
• JAK2 Reflex for Polycythemia with Interpretation, Whole Blood*
• JAK2 Reflex for Polycythemia with Interpretation, Bone Marrow Aspirate*
• MPL codon 515 Mutation, Bone Marrow Aspirate
• MPL codon 515 Mutation, Blood
• MYD88 Exon 5 Sequencing, Tissue, Blood and Bone Marrow
• NRAS Mutation Analysis with Interpretation (Exons 2-4), Tissue
• PML-RARA (t(15:17)) RNA Quantitation with Interpretation, Bone Marrow Aspirate, Peripheral Blood
• TRG Gene Clonality by PCR with Interpretation, Tissue, Blood and Bone Marrow
• *Click on the individual test entry for a comprehensive list of genes in panels

Molecular Genetics General Consult Requisition

• Dystroglycanopathy Mutation Profile
• Factor 5 Leiden/Factor 2 Gene PCR Assay
• Fragile X, DNA Testing
  • FMR1-Related Disorders
  • Premature Ovarian Failure
  • Fragile X Syndrome
  • Fragile X-Associated Tremor/Ataxia Syndrome
• Hemochromatosis, DNA Testing

FSHD Testing

• FSHD - Detection of Abnormal Alleles (FSHD1 and FSHD2)
  (FSHD1 and FSHD2 Requisition) / (FSHD1 and FSHD2 International Requisition)
• FSHD - Prenatal Detection of Abnormal Alleles
  (Prenatal Facioscapulohumeral Dystrophy (FSHD) Molecular Genetics Requisition)
  (Prenatal (Facioscapulohumeral Dystrophy (FSHD) Molecular Genetics International Requisition)

Muscular Dystrophy Molecular Genetics Requisition / International Requisition

• Facioscapulohumeral Dystrophy (FSHD)