Need help choosing the right code?
Ask CasePilot about procedures, modifiers, bundling, and coding guidance.
Try CasePilot© Copyright 2026 American Medical Association. All rights reserved.
The CPT® Code 83914 refers to a specialized laboratory procedure used in molecular genetics to identify mutations or abnormalities within a specific segment of DNA. This process involves the analysis of a molecular sequence, which is a precise arrangement of nucleotides that make up the genetic material. The primary goal of this procedure is to detect mutations that may be associated with various genetic disorders or conditions. The techniques utilized in this code include enzymatic ligation or primer extension methods, which are critical for accurately pinpointing the location of the mutation. Examples of these techniques include the oligonucleotide ligation assay (OLA), single base chain extension (SBCE), and allele-specific primer extension (ASPE). Each of these methods allows for the examination of a single segment of DNA, providing valuable information for genetic testing and research. This procedure is essential for clinicians and researchers who require detailed insights into genetic variations that may impact patient care or contribute to the understanding of hereditary diseases.
© Copyright 2026 Coding Ahead. All rights reserved.
The procedure associated with CPT® Code 83914 is indicated for the identification of specific mutations or abnormalities in genetic material. This analysis is crucial in various clinical and research settings, particularly for the following conditions:
The procedure for CPT® Code 83914 involves several key steps to ensure accurate mutation identification. Each step is critical for the successful analysis of the DNA segment.
After the completion of the procedure associated with CPT® Code 83914, the results are compiled and interpreted by laboratory professionals. The findings are then communicated to the requesting physician, who will use the information to guide clinical decisions. It is important to note that the interpretation of the results may require additional context regarding the patient's clinical history and other diagnostic tests. Patients may also need counseling regarding the implications of the findings, especially if a genetic mutation is identified that could affect their health or that of their family members. Follow-up testing or additional genetic counseling may be recommended based on the results obtained.
| Short Descr | MUTATION IDENT OLA/SBCE/ASPE | Medium Descr | MUTATION ID ENZYMATIC LIG/PRIMER XTN 1 SGM EA | Long Descr | Mutation identification by enzymatic ligation or primer extension, single segment, each segment (eg, oligonucleotide ligation assay [OLA], single base chain extension [SBCE], or allele-specific primer extension [ASPE]) | Status Code | Statutory Exclusion (from MPFS, may be paid under other methodologies) | Global Days | XXX - Global Concept Does Not Apply | PC/TC Indicator (26, TC) | 9 - Not Applicable | Multiple Procedures (51) | 9 - Concept does not apply. | Bilateral Surgery (50) | 9 - Concept does not apply. | Physician Supervisions | 09 - Concept does not apply. | Assistant Surgeon (80, 82) | 9 - Concept does not apply. | Co-Surgeons (62) | 9 - Concept does not apply. | Team Surgery (66) | 9 - Concept does not apply. | Diagnostic Imaging Family | 99 - Concept Does Not Apply | APC Status Indicator | Discontinued Code | Type of Service (TOS) | 5 - Diagnostic Laboratory | Berenson-Eggers TOS (BETOS) | none | MUE | Not applicable/unspecified. | CCS Clinical Classification | 233 - Laboratory - Chemistry and Hematology |
Get instant expert-level medical coding assistance.