UCSF Molecular Diagnostics Laboratory
- GTR Test IDHelpEach Test is a specific, orderable test from a particular laboratory, and is assigned a unique GTR accession number. The format is GTR00000001.1, with a leading prefix 'GTR' followed by 8 digits, a period, then 1 or more digits representing the version. When a laboratory updates a registered test, a new version number is assigned.: GTR000600647.1
- Last updated: 2022-10-27
- Annual Review past due read more
- Test version history
- 600647.1, last updated: 2022-10-27
Clinical testHelpIn the U.S., clinical tests must be performed under CLIA certification. When a lab uses the same methods for a test in both clinical and research settings, the test appears as two separate GTR records. for Acute myeloid leukemia
Offered by UCSF Molecular Diagnostics Laboratory
Overview
Test name
HelpThe name the laboratory assigns the test. Used as the default title of the page specific to the test.UCSF Molecular Diagnostics Laboratory (UCSF MDx)
This is a clinical test intended for HelpPurposes or indications for the test. Lab-provided.: Diagnosis, Monitoring, Prognostic
Click Indication tab for more information.
Blood: 3 mL
Bone marrow aspirate: 3 mL
FFPE: 10 micron sections x5 on uncharged, unstained, glass slides
Germline Sample: Collect 4-6 cytobrushes/cotton swabs on each side of the mouth, place swabs in transport tubes, 2 swabs per tube.
Order URL HelpLink to the laboratory webpage with information about how to order this test. Please note that clicking on this link will open a new tab in your internet browser.: https://www.testmenu.com/UCSFClinLab/Tests/1101200
Specimen source
Methodology
HelpThe assay's major method category (biochemical, cytogenetic or molecular genetics); method category (i.e. enzyme assay, chromosome breakage studies, targeted mutation analysis); methodology (i.e. the name of the method used) and instruments used when performing this test.- Molecular Genetics
- CSequence analysis of the entire coding region
- Next-Generation (NGS)/Massively parallel sequencing (MPS)
- Illumina MiSeq
Not provided
Clinical validity
HelpHow consistently and accurately the test detects or predicts the intermediate or final outcomes of interest. Lab-provided.Not provided
Test services
HelpLaboratory's order or catalog code for the test (used in the order requisition form).- Clinical Testing/Confirmation of Mutations Identified Previously
- NCCN, 2024NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) Acute Lymphoblastic Leukemia, 2024
- NCCN, 2023NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) Acute Myeloid Leukemia, 2023
- NCCN, 2011NCCN Task Force report: Evaluating the clinical utility of tumor markers in oncology.
- OMIM
- View RUNX1 variations in ClinVar
- View CEBPA variations in ClinVar
- View DNMT3A variations in ClinVar
- View ETV6 variations in ClinVar
- View FLT3 variations in ClinVar
- View GATA2 variations in ClinVar
- View JAK2 variations in ClinVar
- View KIT variations in ClinVar
- View KRAS variations in ClinVar
- View LPP variations in ClinVar
- View NPM1 variations in ClinVar
- View SH3GL1 variations in ClinVar
- View TERT variations in ClinVar
- View NUP214 variations in ClinVar
- View MLLT10 variations in ClinVar
- View PICALM variations in ClinVar
- View CHIC2 variations in ClinVar
- RefSeqGene
- Coriell Institute for Medical Research
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