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Analysis of HBA1/HBA2 genes for duplications and deletions, associated with alpha thalassemia.
2025 CPT code 81203
Analysis of the APC gene for duplication/deletion variants.
2025 CPT code 81301
Microsatellite instability analysis to detect mismatch repair deficiency, including comparison of neoplastic and normal tissue if performed.
2025 CPT code 81182
Analysis of the ATXN8OS gene to detect abnormal alleles, specifically expanded sequences, often associated with spinocerebellar ataxia 8 (SCA8).
2025 CPT code 81292
Complete gene sequencing analysis of the MLH1 gene.
2025 CPT code 81297
Analysis of the MSH2 gene for duplications and deletions.
2025 CPT code 81200
Analysis of the ASPA gene for common variants (e.g., E285A, Y231X).
2025 CPT code 81403
This CPT code represents the technical component of a Tier 2, Level 4 molecular pathology procedure.It encompasses various analyses of a single gene, including DNA sequencing, multiplex PCR, mutation scanning, or duplication/deletion variant analysis.
2025 CPT code 81296
Analysis of known familial variants in the MSH2 gene.
2025 CPT code 81111
Analysis of the common alleles of Human Platelet Antigen 9 (HPA-9) gene.
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).
2025 CPT code 81258
HBA1/HBA2 (alpha globin 1 and alpha globin 2) gene analysis for known familial variants.
2025 CPT code 81163
BRCA1 and BRCA2 gene analysis; full sequence analysis.
2025 CPT code 81217
BRCA2 (BRCA2, DNA repair associated) (eg, hereditary breast and ovarian cancer) gene analysis; known familial variant
2025 CPT code 81255
HEXA (hexosaminidase A [alpha polypeptide]) (eg, Tay-Sachs disease) gene analysis, common variants (eg, 1278insTATC, 1421+1G>C, G269S).
2025 CPT code 81331
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.
High-resolution HLA Class I typing for a single allele or allele group.
2025 CPT code 81112
Analysis of the common alleles of Human Platelet Antigen 15 (HPA-15), also known as CD109 (CD109 molecule), using a blood or amniotic fluid specimen.
2025 CPT code 81370
HLA Class I and II typing, low resolution, molecular techniques.
2025 CPT code 81109
Analysis of common Human Platelet Antigen 5 (HPA-5) gene variants (e.g., HPA-5a/b [K505E]) using a patient specimen (e.g., blood).
2025 CPT code 81332
Analysis of common SERPINA1 gene variants (e.g., *S and *Z) associated with alpha-1-antitrypsin deficiency.
2025 CPT code 81345
Analysis of the telomerase reverse transcriptase (TERT) gene, focusing on targeted sequences like the promoter region.
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