Hereditary Pancreatic Cancer Panel, Sequencing and Deletion/Duplication

Casandra

Casandra Test Code AR64233Version 1 (DRAFT)

Performing Lab

Lab ARUP LaboratoriesLab Test ID 3005708CPT Code 81432

Hereditary Pancreatic Cancer Panel, Sequencing and Deletion/Duplication

Also known as: PANCAN NGS

Clinical Use

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Use

This test is recommended to confirm a hereditary cause of pancreatic cancer in individuals with a personal or family history. Pathogenic germline variants in multiple genes have been implicated in hereditary pancreatic cancer. Hereditary cancer syndromes are often characterized by early age of cancer onset (typically before 50 years of age) and multiple, multifocal, and/or similar cancers in a single individual or in a closely related family member(s).

Special Instructions

Testing minors for adult-onset conditions is not recommended; testing will not be performed in minors without prior approval. For additional information, please contact an ARUP genetic counselor at 800-242-2787 ext. 2141. Counseling and informed consent are recommended for genetic testing. Consent forms are available online.

Limitations

A negative result does not exclude a heritable form of cancer. This test only detects variants within the coding regions and intron-exon boundaries of the targeted genes. Deletions/duplications/insertions of any size may not be detected by massively parallel sequencing. Regulatory region variants and deep intronic variants will not be identified. Precise breakpoints for large deletions or duplications are not determined in this assay and single exon deletions/duplications may not be detected based on the breakpoints of the rearrangement.

Test Details