Last updated: October 2026CMS rates · Free lookup
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Related codes
81383Transplant Match Genetic Test, A Lab Analysis That Identifies The Type Of Human Leukocyte Antigen (Hla). The Result Is Used To Identify The Best Donor And Recipient For Bone Marrow Or Cord Blood.
$109.1381401Mopath Procedure Level 2, Molecular Pathology Procedure Level 2 (Eg 2-10 Snps 1 Methylated Variant Or 1 Somatic Variant [Typically Using Nonsequencing Target Variant Analysis] Or Detection Of A Dynamic Mutation Disorder Triplet Repeat) Abcc8 (Atp-Binding Cassette Sub-Family C [Cftr Mrp] Member 8) (Eg Familial Hyperinsulinism) Common Variants (Eg C.3898-9g>A [C.3992-9g>A] F1388del) Abl1 (Abl Proto-Oncogene 1 Non-Receptor Tyrosine Kinase) (Eg Acquired Imatinib Resistance) T315i Variant Acadm (Acyl-Coa Dehydrogenase C-4 To C-12 Straight Chain Mcad) (Eg Medium Chain Acyl Dehydrogenase Deficiency) Commons Variants (Eg K304e Y42h) Adrb2 (Adrenergic Beta-2 Receptor Surface) (Eg Drug Metabolism) Common Variants (Eg G16r Q27e) Apob (Apolipoprotein B) (Eg Familial Hypercholesterolemia Type B) Common Variants (Eg R3500q R3500w) Apoe (Apolipoprotein E) (Eg Hyperlipoproteinemia Type Iii Cardiovascular Disease Alzheimer Disease) Common Variants (Eg *2 *3 *4) Cbfb Myh11 (Inv(16)) (Eg Acute Myeloid Leukemia) Qualitative And Quantitative If Performed Cbs (Cystathionine-Beta-Synthase) (Eg Homocystinuria Cystathionine Beta-Synthase Deficiency) Common Variants (Eg I278t G307s) Cfh Arms2 (Complement Factor H Age-Related Maculopathy Susceptibility 2) (Eg Macular Degeneration) Common Variants (Eg Y402h [Cfh] A69s [Arms2]) Dek Nup214 (T(6 9)) (Eg Acute Myeloid Leukemia) Translocation Analysis Qualitative And Quantitative If Performed E2a Pbx1 (T(1 19)) (Eg Acute Lymphocytic Leukemia) Translocation Analysis Qualitative And Quantitative If Performed Eml4 Alk (Inv(2)) (Eg Non-Small Cell Lung Cancer) Translocation Or Inversion Analysis Etv6 Runx1 (T(12 21)) (Eg Acute Lymphocytic Leukemia) Translocation Analysis Qualitative And Quantitative If Performed Ewsr1 Atf1 (T(12 22)) (Eg Clear Cell Sarcoma) Translocation Analysis Qualitative And Quantitative If Performed Ewsr1 Erg (T(21 22)) (Eg Ewing Sarcoma Peripheral Neuroectodermal Tumor) Translocation Analysis Qualitative And Quantitative If Performed Ewsr1 Fli1 (T(11 22)) (Eg Ewing Sarcoma Peripheral Neuroectodermal Tumor) Translocation Analysis Qualitative And Quantitative If Performed Ewsr1 Wt1 (T(11 22)) (Eg Desmoplastic Small Round Cell Tumor) Translocation Analysis Qualitative And Quantitative If Performed F11 (Coagulation Factor Xi) (Eg Coagulation Disorder) Common Variants (Eg E117x [Type Ii] F283l [Type Iii] Ivs14del14 And Ivs14+1g>A [Type I]) Fgfr3 (Fibroblast Growth Factor Receptor 3) (Eg Achondroplasia Hypochondroplasia) Common Variants (Eg 1138g>A 1138g>C 1620c>A 1620c>G) Fip1l1 Pdgfra (Del[4q12]) (Eg Imatinib-Sensitive Chronic Eosinophilic Leukemia) Qualitative And Quantitative If Performed Flg (Filaggrin) (Eg Ichthyosis Vulgaris) Common Variants (Eg R501x 2282del4 R2447x S3247x 3702delg) Foxo1 Pax3 (T(2 13)) (Eg Alveolar Rhabdomyosarcoma) Translocation Analysis Qualitative And Quantitative If Performed Foxo1 Pax7 (T(1 13)) (Eg Alveolar Rhabdomyosarcoma) Translocation Analysis Qualitative And Quantitative If Performed Fus Ddit3 (T(12 16)) (Eg Myxoid Liposarcoma) Translocation Analysis Qualitative And Quantitative If Performed Galc (Galactosylceramidase) (Eg Krabbe Disease) Common Variants (Eg C.857g>A 30-Kb Deletion) Galt (Galactose-1-Phosphate Uridylyltransferase) (Eg Galactosemia) Common Variants (Eg Q188r S135l K285n T138m L195p Y209c Ivs2-2a>G P171s Del5kb N314d L218l N314d) H19 (Imprinted Maternally Expressed Transcript [Non-Protein Coding]) (Eg Beckwith-Wiedemann Syndrome) Methylation Analysis Igh@ Bcl2 (T(14 18)) (Eg Follicular Lymphoma) Translocation Analysis Single Breakpoint (Eg Major Breakpoint Region [Mbr] Or Minor Cluster Region [Mcr]) Qualitative Or Quantitative (When Both Mbr And Mcr Breakpoints Are Performed Use 81278) Kcnq1ot1 (Kcnq1 Overlapping Transcript 1 [Non-Protein Coding]) (Eg Beckwith-Wiedemann Syndrome) Methylation Analysis Linc00518 (Long Intergenic Non-Protein Coding Rna 518) (Eg Melanoma) Expression Analysis Lrrk2 (Leucine-Rich Repeat Kinase 2) (Eg Parkinson Disease) Common Variants (Eg R1441g G2019s I2020t) Med12 (Mediator Complex Subunit 12) (Eg Fg Syndrome Type 1 Lujan Syndrome) Common Variants (Eg R961w N1007s) Meg3 Dlk1 (Maternally Expressed 3 [Non-Protein Coding] Delta-Like 1 Homolog [Drosophila]) (Eg Intrauterine Growth Retardation) Methylation Analysis Mll Aff1 (T(4 11)) (Eg Acute Lymphoblastic Leukemia) Translocation Analysis Qualitative And Quantitative If Performed Mll Mllt3 (T(9 11)) (Eg Acute Myeloid Leukemia) Translocation Analysis Qualitative And Quantitative If Performed Mt-Atp6 (Mitochondrially Encoded Atp Synthase 6) (Eg Neuropathy With Ataxia And Retinitis Pigmentosa [Narp] Leigh Syndrome) Common Variants (Eg M.8993t>G M.8993t>C) Mt-Nd4 Mt-Nd6 (Mitochondrially Encoded Nadh Dehydrogenase 4 Mitochondrially Encoded Nadh Dehydrogenase 6) (Eg Leber Hereditary Optic Neuropathy [Lhon]) Common Variants (Eg M.11778g>A M.3460g>A M.14484t>C) Mt-Nd5 (Mitochondrially Encoded Trna Leucine 1 [Uua G] Mitochondrially Encoded Nadh Dehydrogenase 5) (Eg Mitochondrial Encephalopathy With Lactic Acidosis And Stroke-Like Episodes [Melas]) Common Variants (Eg M.3243a>G M.3271t>C M.3252a>G M.13513g>A) Mt-Rnr1 (Mitochondrially Encoded 12s Rna) (Eg Nonsyndromic Hearing Loss) Common Variants (Eg M.1555a>G M.1494c>T) Mt-Tk (Mitochondrially Encoded Trna Lysine) (Eg Myoclonic Epilepsy With Ragged-Red Fibers [Merrf]) Common Variants (Eg M.8344a>G M.8356t>C) Mt-Tl1 (Mitochondrially Encoded Trna Leucine 1 [Uua G]) (Eg Diabetes And Hearing Loss) Common Variants (Eg M.3243a>G M.14709 T>C) Mt-Tl1 Mt-Ts1 Mt-Rnr1 (Mitochondrially Encoded Trna Serine 1 [Ucn] Mitochondrially Encoded 12s Rna) (Eg Nonsyndromic Sensorineural Deafness [Including Aminoglycoside-Induced Nonsyndromic Deafness]) Common Variants (Eg M.7445a>G M.1555a>G) Mutyh (Muty Homolog [E. Coli]) (Eg Myh-Associated Polyposis) Common Variants (Eg Y165c G382d) Nod2 (Nucleotide-Binding Oligomerization Domain Containing 2) (Eg Crohns Disease Blau Syndrome) Common Variants (Eg Snp 8 Snp 12 Snp 13) Npm1 Alk (T(2 5)) (Eg Anaplastic Large Cell Lymphoma) Translocation Analysis Pax8 Pparg (T(2 3) (Q13 P25)) (Eg Follicular Thyroid Carcinoma) Translocation Analysis Prame (Preferentially Expressed Antigen In Melanoma) (Eg Melanoma) Expression Analysis Prss1 (Protease Serine 1 [Trypsin 1]) (Eg Hereditary Pancreatitis) Common Variants (Eg N29i A16v R122h) Pygm (Phosphorylase Glycogen Muscle) (Eg Glycogen Storage Disease Type V Mcardle Disease) Common Variants (Eg R50x G205s) Runx1 Runx1t1 (T(8 21)) (Eg Acute Myeloid Leukemia) Translocation Analysis Qualitative And Quantitative If Performed Ss18 Ssx1 (T(X 18)) (Eg Synovial Sarcoma) Translocation Analysis Qualitative And Quantitative If Performed Ss18 Ssx2 (T(X 18)) (Eg Synovial Sarcoma) Translocation Analysis Qualitative And Quantitative If Performed Vwf (Von Willebrand Factor) (Eg Von Willebrand Disease Type 2n) Common Variants (Eg T791m R816w R854q)
$137.00Methodology
Rates come from the CMS Clinical Laboratory Fee Schedule (CLFS), published quarterly. Each HCPCS payment amount reflects the national CLFS payment for outpatient laboratory services.
View CMS Clinical Laboratory Fee Schedule