81321 Pten gene full sequence
Also known as: PTEN full sequencing, Cowden syndrome genetic test
Phosphatase and Tensin Homolog (PTEN) gene full gene sequence analysis to identify variants associated with Cowden syndrome.
In Plain Language
Hereditary cancer predisposition test; Multiple hamartoma syndrome screening
Clinical Context
Full PTEN sequencing for Cowden syndrome and PTEN-related disorders with increased risk of breast, thyroid, and other cancers.
RVU Information
CPT 81321 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 81321?
CPT 81321 (Pten gene full sequence) is a Pathology & Lab code. Phosphatase and Tensin Homolog (PTEN) gene full gene sequence analysis to identify variants associated with Cowden syndrome.
Who uses CPT code 81321?
CPT 81321 is used by Pathology, Oncology, Genetics. Full PTEN sequencing for Cowden syndrome and PTEN-related disorders with increased risk of breast, thyroid, and other cancers.
When is CPT 81321 used?
Full PTEN sequencing for Cowden syndrome and PTEN-related disorders with increased risk of breast, thyroid, and other cancers.
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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.