81347 Sf3b1 gene common variants
Also known as: SF3B1 variant testing, splicing mutation analysis
Splicing Factor 3B Subunit 1 (SF3B1) gene analysis for common variants in hematologic malignancies.
In Plain Language
Blood cancer mutation test; Leukemia genetic marker
Clinical Context
Detects SF3B1 mutations in acute myeloid leukemia, myelodysplastic syndrome, and other hematologic malignancies.
RVU Information
CPT 81347 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 81347?
CPT 81347 (Sf3b1 gene common variants) is a Pathology & Lab code. Splicing Factor 3B Subunit 1 (SF3B1) gene analysis for common variants in hematologic malignancies.
Who uses CPT code 81347?
CPT 81347 is used by Pathology, Hematology, Oncology. Detects SF3B1 mutations in acute myeloid leukemia, myelodysplastic syndrome, and other hematologic malignancies.
When is CPT 81347 used?
Detects SF3B1 mutations in acute myeloid leukemia, myelodysplastic syndrome, and other hematologic malignancies.
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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.