Breast Actionable Hereditary Gene Analysis Deletion and Duplication

Sunquest Code:BRCACT  
Epic Code:LAB6950Epic Name:Hereditary Cancer Breast Actionable
Synonyms:BreastPlus; BRCA1; BRCA2; Hereditary; Breast; Genetic Testing; Hereditary Breast and Ovarian Cancer Syndrome; HBOC; Breast Cancer; Hereditary Breast Cancer; Early Onset Breast Cancer; Ovarian Cancer
Methodology:Next generation sequencing
CPT Code:81408, 81408, 81406, 81479, 81406, 81321, 81405, 81162, 81405, 81479, 81323, G0452
Turnaround Time:Testing is performed Mon-Fri; results are reported within 4-6 weeks.
Special Instructions:Gene(s) or the name of the panel should be indicated in the comment section of EPIC order.
A signed informed consent in the patient's medical record is required; the consent should not be sent to the laboratory. The link to the Genetic Testing Consent Form is provided as a convenience for the providers and genetic counselors.
Bone Marrow Transplant patients: If a patient is the recipient of an allogeneic transplant, this test must be done on a pre-transplant sample. Contact the Molecular Diagnostics lab to see if a pre-transplant sample is available.
Associated Links:

NGS Genetic Testing Consent Form, MD Hereditary Order Instructions

Collection Instructions

Optimal Volume:10 mL
Minimum\Peds Volume:3 mL
Container:Yellow (ACD, Solution A) tube available from laboratory (Purple (EDTA))
Causes for Rejection:Frozen or clotted specimen, incorrect anticoagulant, specimen more than 5 days old. Sample collected from bone marrow transplant recipient. Samples tested in hematology using automated instrumentation not accepted. DNA extracted at non-CLIA certified (or equivalent) lab.

Processing and Shipping

Specimen Processing:Do not process. Store at room temperature.
Shipping Instructions:Ship at room temperature.
Test Performed at or Referral Lab Molecular Diagnostics  (UMMC-East Bank)


Reference Range:By report.
Use:The Breast Actionable cancer panel is a genetic test which analyzes 11 genes known to be associated with an increased lifetime risk of breast and other cancers. Published medical guidelines exist for detection, prevention, risk reduction and/or treatment of individuals with mutations in these genes.This assay utilizes a next generation sequencing (NGS) platform. This platform allows simultaneous sequencing of a large number of genes using a single assay. Genomic DNA is extracted from the sample, and the sequencing libraries are prepared according to standard Illumina protocols using the TruSight One Sequencing Panel for enrichment of targeted genes. The enriched DNA libraries are sequenced on an Ilumina HiSeq 2500 instrument. Raw sequencing reads are mapped to the reference genome using BWA. Raw alignment files are realigned in the neighborhood of indels, and recalibrated for base quality accuracy using the Genome Analysis Tool Kit (GATK) Point mutation and indel calls in exons and adjoining intronic regions are made using the GATK Unified Genotyper. Variants are interpreted according to guidance issued by the American College of Medical Genetics.

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