Upgrade for detailed insurance, legislation, and other documents analytics for individual cases; real-time analysis of the datasets from your EHR, CRM, ERP, or other software; and more Enterprise Features.
Methylation analysis of SNRPN and UBE3A genes (e.g., for Prader-Willi and/or Angelman syndromes).
2025 CPT code 81232
Analysis of common variants in the dihydropyrimidine dehydrogenase (DPYD) gene (e.g., *2A, *4, *5, *6) to assess drug metabolism, primarily for 5-fluorouracil (5-FU) and capecitabine.
2025 CPT code 81246
Analysis of FLT3 gene for tyrosine kinase domain (TKD) variants.
2025 CPT code 81361
Analysis of the HBB gene for common variants (e.g., HbS, HbC, HbE).
2025 CPT code 81194
Analysis of NTRK1, NTRK2, and NTRK3 gene translocations.
2025 CPT code 81178
Analysis of the ATXN1 gene to detect abnormal alleles, specifically expanded sequences, often associated with spinocerebellar ataxia type 1 (SCA1).
2025 CPT code 81208
Analysis of BCR/ABL1 gene sequences at breakpoints other than major or minor, qualitative or quantitative.
2025 CPT code 81259
Full gene sequence analysis of HBA1/HBA2 genes (alpha globin 1 and alpha globin 2) related to alpha thalassemia and some hemoglobinopathies.
2025 CPT code 81164
BRCA1 and BRCA2 gene analysis; full duplication/deletion analysis.
2025 CPT code 81183
Analysis of the ATXN10 gene to detect abnormal alleles, particularly expanded sequences.
2025 CPT code 81257
Analysis of HBA1/HBA2 genes (alpha globin 1 and 2) for common deletions or variants associated with alpha thalassemia and other hemoglobinopathies.
2025 CPT code 81242
Analysis of the FANCC gene for common variants, such as IVS4+4A>T, associated with Fanconi anemia.
2025 CPT code 81317
Analysis of the entire PMS2 gene sequence.
2025 CPT code 81204
Analysis of the androgen receptor (AR) gene to characterize alleles, such as expanded size or methylation status.
2025 CPT code 81291
Analysis of common variants in the MTHFR gene.
2025 CPT code 81108
This code represents Human Platelet Antigen 4 (HPA-4) genotyping, analyzing common variants HPA-4a/b (R143Q) in the ITGB3 gene.The test aids in diagnosing conditions such as neonatal alloimmune thrombocytopenia (NAIT).
2025 CPT code 81248
Analysis of known familial variants in the glucose-6-phosphate dehydrogenase (G6PD) gene.
2025 CPT code 81231
Analysis of common CYP3A5 gene variants (*2, *3, *4, *5, *6, *7) impacting drug metabolism.
2025 CPT code 81229
Cytogenomic (genome-wide) microarray analysis for constitutional chromosomal abnormalities; interrogation of genomic regions for copy number and single nucleotide polymorphism (SNP) variants.
2025 CPT code 81355
Analysis of VKORC1 gene for common variants related to warfarin metabolism.
2025 CPT code 81210
BRAF (B-Raf proto-oncogene, serine/threonine kinase) gene analysis for V600 variant(s).
2025 CPT code 81383
HLA Class II typing, high resolution (ie, alleles or allele groups); one allele or allele group (eg, HLA-DQB1*06:02P), each
F9 (coagulation factor IX) (eg, hemophilia B), full gene sequence
2025 CPT code 81230
Analysis of the CYP3A4 gene for common variants (e.g., *2, *22) to assess drug metabolism.
2025 CPT code 81247
G6PD (glucose-6-phosphate dehydrogenase) (eg, hemolytic anemia, jaundice), gene analysis; common variant(s) (eg, A, A-)
2025 CPT code 81329
SMN1 (survival of motor neuron 1, telomeric) (e.g., spinal muscular atrophy) gene analysis; dosage/deletion analysis (e.g., carrier testing), includes SMN2 (survival of motor neuron 2, centromeric) analysis, if performed.
2025 CPT code 81357
U2AF1 (U2 small nuclear RNA auxiliary factor 1) gene analysis, common variants (e.g., S34F, S34Y, Q157R, Q157P).
PML/RARalpha,(t(15;17)), (promyelocytic leukemia/retinoic acid receptor alpha) (eg, promyelocytic leukemia) translocation analysis; single breakpoint (eg, intron 3, intron 6 or exon 6), qualitative or quantitative. (For intron 3 and intron 6 [including exon 6 if performed] analysis, use 81315). (If both intron 6 and exon 6 are analyzed, without intron 3, use one unit of 81316)
2025 CPT code 81315
PML/RARalpha,(t(15;17)), (promyelocytic leukemia/retinoic acid receptor alpha) (eg, promyelocytic leukemia) translocation analysis; common breakpoints (eg, intron 3 and intron 6), qualitative or quantitative
2025 CPT code 81275
KRAS (Kirsten rat sarcoma viral oncogene homolog) (eg, carcinoma) gene analysis; variants in exon 2 (eg, codons 12 and 13)
2025 CPT code 81380
HLA Class I typing, high resolution (ie, alleles or allele groups); one locus (eg, HLA-A, -B, or -C), each.
2025 CPT code 81402
Molecular pathology procedure, level 3.This includes analysis of >10 single nucleotide polymorphisms (SNPs), 2-10 methylated variants, 2-10 somatic variants, immunoglobulin and T-cell receptor gene rearrangements, duplication/deletion variants of one exon, loss of heterozygosity (LOH), and uniparental disomy (UPD).
2025 CPT code 81278
IGH@/BCL2 (t(14;18)) (eg, follicular lymphoma) translocation analysis, major breakpoint region (MBR) and minor cluster region (mcr) breakpoints, qualitative or quantitative.
2025 CPT code 81408
Molecular pathology procedure, Level 9 (eg, analysis of >50 exons in a single gene by DNA sequence analysis).
BRCA2 (BRCA2, DNA repair associated) (eg, hereditary breast and ovarian cancer) gene analysis; full duplication/deletion analysis (ie, detection of large gene rearrangements).
CSTB (cystatin B) (eg, Unverricht-Lundborg disease) gene analysis; evaluation to detect abnormal (eg, expanded) alleles
Continue with Personal Account
Thank you for exploring iFrame ♥ Please subscribe for unlimited access to our top-tier AI model, which directly supports our dedicated knowledge creators maintaining an ad-free internet experience.