Test ID: CFTRM
CFTR Gene, Full Gene Analysis
List Fee
Provides the Mayo Medical Laboratories list fee for performing the test
$1796.90
The following test(s) will be added at an additional charge:
$289.60 for #89852 CFTR Large Deletion/Duplication, MLPA
$2,086.50 = Total List Fee
Test Classification
Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer's instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR), Investigation Use Only (IUO) product, or a Research Use Only (RUO) product.
CPT Code Information
Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Medical Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.
CFTR Gene, Full Gene Analysis
81223-CFTR (cystic fibrosis transmembrane conductance regulator) (eg, cystic fibrosis) gene analysis; full gene sequence
CFTR Large Deletion/Duplication, MLPA
81222-CFTR (cystic fibrosis transmembrane conductance regulator) (eg, cystic fibrosis) gene analysis; duplication/deletion variants
For nonparticipating payers:
CFTR Gene, Full Gene Analysis
83891-Isolation or extraction of highly purified nucleic acid
83892 x 8-Enzymatic digestion
83894 x 8-Separation by gel electrophoresis
83900 x 8-Amplification, target, multiplex, first 2 nucleic acid sequences
83901 x 11-Amplification, target, multiplex, each additional nucleic acid sequence beyond 2
83909 x 56-Separation and identification by high-resolution technique
83912-Interpretation and report
CFTR Large Deletion/Duplication, MLPA
83900-Amplification, target, multiplex, first 2 nucleic acid sequences
83909-Separation and identification by high-resolution technique
83914 x 31-Mutation identification by enzymatic ligation or primer extension, single segment, each segment


