Casandra
Casandra Test Code NG26032Version 1 (DRAFT)
Performing Lab
BRCA1 Single Gene (Germline)
Clinical Use
Order TestUse
This test analyzes the BRCA1 gene for germline variants, specifically small sequence variants such as SNVs and indels, through DNA sequencing to detect pathogenic or likely pathogenic variants relevant to inherited breast and ovarian cancer risk. The information supports clinical decision-making regarding risk assessment, early detection, family counseling, and potential preventive measures.
Special Instructions
Testing is performed by Fulgent Genetics as a send-out. Samples must be transported with a cold pack not in direct contact with the specimen. For New York State clients, please provide date and time of collection.
Limitations
Not provided.
Test Details
Methodology
NGS
Biomarkers
BRCA1
GeneSNV/Indel • Mutation • Categorical (e.g., Positive / Negative / Indeterminate)
Result Turnaround Time
Not provided.
Related Documents
For more information, please review the documents below
Specimen Requirements
Specimen
Whole Blood
Volume
two x 4 mL
Minimum Volume
Not provided
Container
EDTA tube
