81292 Mlh1 gene full seq
Also known as: MLH1 full sequencing, MLH1 complete gene analysis
Mutator S Homolog 1 (MLH1) gene full gene sequence analysis to identify all mutation types associated with Lynch syndrome.
In Plain Language
Complete Lynch syndrome gene test; Full colorectal cancer genetic screening
Clinical Context
Complete MLH1 sequencing for Lynch syndrome diagnosis when initial testing is negative or uncertain. Detects all variant types.
RVU Information
CPT 81292 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 81292?
CPT 81292 (Mlh1 gene full seq) is a Pathology & Lab code. Mutator S Homolog 1 (MLH1) gene full gene sequence analysis to identify all mutation types associated with Lynch syndrome.
Who uses CPT code 81292?
CPT 81292 is used by Pathology, Oncology, Gastroenterology. Complete MLH1 sequencing for Lynch syndrome diagnosis when initial testing is negative or uncertain. Detects all variant types.
When is CPT 81292 used?
Complete MLH1 sequencing for Lynch syndrome diagnosis when initial testing is negative or uncertain. Detects all variant types.
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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.