81357 U2af1 gene common variants
Also known as: U2AF1 variant testing, splicing factor mutation analysis
U2-Dependent Splicing Factor U2AF1 (U2AF1) gene analysis for common variants in hematologic malignancies.
In Plain Language
Blood cancer mutation test; Myelodysplastic syndrome marker
Clinical Context
Detects U2AF1 mutations in myelodysplastic syndrome and acute myeloid leukemia for prognosis and monitoring.
RVU Information
CPT 81357 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 81357?
CPT 81357 (U2af1 gene common variants) is a Pathology & Lab code. U2-Dependent Splicing Factor U2AF1 (U2AF1) gene analysis for common variants in hematologic malignancies.
Who uses CPT code 81357?
CPT 81357 is used by Pathology, Hematology, Oncology. Detects U2AF1 mutations in myelodysplastic syndrome and acute myeloid leukemia for prognosis and monitoring.
When is CPT 81357 used?
Detects U2AF1 mutations in myelodysplastic syndrome and acute myeloid leukemia for prognosis and monitoring.
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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.