Start New EnglishEspañol中文РусскийالعربيةTiếng ViệtFrançaisDeutsch한국어Tagalog Library Performance
ALL MEDICAL CODES IN CATEGORY Tier 1 Molecular Pathology Procedures, Genetic Analysis Procedures

2025 CPT code 81331

Methylation analysis of SNRPN and UBE3A genes (e.g., for Prader-Willi and/or Angelman syndromes).

2025 CPT code 81338

Analysis of common MPL gene variants (e.g., W515A, W515K, W515L, W515R) associated with myeloproliferative neoplasms.

2025 CPT code 81326

Analysis of the PMP22 gene for known familial variants associated with conditions like Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies.

2025 CPT code 81192

Analysis of NTRK2 (neurotrophic receptor tyrosine kinase 2) gene translocations, often associated with certain solid tumors.

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 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 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 81194

Analysis of NTRK1, NTRK2, and NTRK3 gene translocations.

2025 CPT code 81265

Comparative analysis using Short Tandem Repeat (STR) markers; patient and comparative specimen (e.g., pre-transplant recipient and donor germline testing, post-transplant non-hematopoietic recipient germline [e.g., buccal swab or other germline tissue sample] and donor testing, twin zygosity testing, or maternal cell contamination of fetal cells).

2025 CPT code 81236

Analysis of the entire EZH2 gene sequence.

2025 CPT code 81362

Analysis of the HBB gene for known familial variants.

2025 CPT code 81164

BRCA1 and BRCA2 gene analysis; full duplication/deletion analysis.

2025 CPT code 81311

Analysis of NRAS gene variants in exons 2 and 3.

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.