81165 Brca1 gene full seq alys
Also known as: BRCA1 sequencing, BRCA1 full analysis
Complete sequence analysis of the BRCA1 gene to identify point mutations and small insertions/deletions associated with hereditary breast and ovarian cancer.
In Plain Language
breast cancer gene test; BRCA1 mutation screening
Clinical Context
Used to comprehensively screen for pathogenic variants in BRCA1 specifically in patients with personal or family history of breast or ovarian cancer for risk stratification.
RVU Information
CPT 81165 does not have a physician work RVU assigned by CMS. Reimbursement for this code is determined by payer-specific fee schedules.
Billing & Documentation
Lab and pathology codes require an order from the treating provider with clinical indication. For molecular pathology and genetic testing, document the specific analytes tested and clinical rationale.
How This Code Compares
This code has a work RVU of 0.00, meaning it does not have a physician work component assigned by CMS. In the Pathology & Lab category, 94% of codes share this characteristic.
Specialties
Frequently Asked Questions
What is CPT code 81165?
CPT 81165 (Brca1 gene full seq alys) is a Pathology & Lab code. Complete sequence analysis of the BRCA1 gene to identify point mutations and small insertions/deletions associated with hereditary breast and ovarian cancer.
Who uses CPT code 81165?
CPT 81165 is used by Oncology, Pathology, Genetics. Used to comprehensively screen for pathogenic variants in BRCA1 specifically in patients with personal or family history of breast or ovarian cancer for risk stratification.
When is CPT 81165 used?
Used to comprehensively screen for pathogenic variants in BRCA1 specifically in patients with personal or family history of breast or ovarian cancer for risk stratification.
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CPT® is a registered trademark of the American Medical Association. Data sourced from CMS Physician Fee Schedule RVU26A. Descriptions, synonyms, and clinical context are original content by RVU Edge.