Sign in →

Test Code NGS50L Myeloid 50 Gene NGS Panel Blood

Additional Test Codes

Epic Order Name: Myeloid 50 Gene NGS Panel Blood
Sunquest Order Code: NGS50L
Px Order Code: LAB3198

Specimen Collection Type

EDTA (lavender-top) tube, 3.0 mL

For bone marrow see: Myeloid 50 Gene NGS Panel Non Blood (NGS50M)

Minimum Collection Volume

Minimum 0.5 mL

Additional Information / Notes

Genes Tested: ABL1, ANKRD26, ASXL1, BCR, BLM, BRAF, CALR, CBL, CEBPA, CSF3R, CUX1, DDX41, DNMT3A, ELANE, ETNK1, ETV6, EZH2, FBXW7, FLT3, GATA2, IDH1, IDH2, IKZF1, JAK2, KIT, KRAS, MPL, MYD88, NF1, NOTCH1, NPM1, NRAS, PAX5, PDGFRA, PTPN11, RUNX1, SETBP1, SF3B1, SH2B3, SRP72, SRSF2, STAG2, STAT3, TERC, TERT, TET2, TP53, U2AF1, WT1, ZRSR2.

Reference Range

An interpretive report will be provided

Critical Value

N/A

Specimen Availability for Add-on Testing

Only for additional testing provided by CMOL; additional sample may be required, see individual test sample requirements and stability.

Specimen Stability

Peripheral Blood: 5 days at 4°C

Day(s) Performed

8:30 AM – 5:00 PM, Monday through Friday; varies

Performing Lab - Department

TUKHS – Molecular Pathology (CMOL)

CPT Code

81479

LOINC Code

N/A

Performing Lab- Department

TUKHS Molecular Pathology (CMOL)

Clinical Indications

Detects somatic small nucleotide variations (SNVs) and small insertions/deletions (INDELs) in 50 genes of importance across various types of hematologic malignancies. Useful for diagnosis support, prognosis, risk stratification,
and informing possible treatment decisions and clinical trials. The presence of gene variants in various cancers can serve as a prognostic indicator and can impact a patient’s response to some anti-cancer therapies, making detection
of gene variants useful in guiding treatment decisions.

Test Alias

N/A

Rejection Criteria

Peripheral Blood: Severely clotted or hemolyzed samples