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Multigene Myeloid Panel
Clinical Genetic Test
Help
offered by
UCSF Molecular Diagnostics Laboratory
View lab's test page
LinkOut
GTR Test Accession: Help GTR000607940.1
CAP
IMMUNOLOGYINHERITED DISEASECANCER ... View more
Registered in GTR: 2023-07-17
View version history
Last annual review date for the lab: 2022-10-27 Past due LinkOut
At a Glance
Test purpose: Help
Diagnosis; Drug Response; Monitoring; ...
Conditions (1): Help
Acute myeloid leukemia
Genes (52): Help
ABL1 (9q34.12); ASXL1 (20q11.21); BCOR (Xp11.4); BCORL1 (Xq26.1); BRAF (7q34) more...
Methods (1): Help
Molecular Genetics - Mutation scanning of select exons: Next-Generation (NGS)/Massively parallel sequencing (MPS)
Target population: Help
Acute myeloid leukemia, myeodysplastic syndromes, primary myelifibrosis
Clinical validity: Help
Not provided
Clinical utility: Help
Not provided
Ordering Information
Offered by: Help
UCSF Molecular Diagnostics Laboratory
View lab's website
View lab's test page
Test short name: Help
MMP
Specimen Source: Help
  • Bone marrow
  • Buccal swab
  • Cell culture
  • Isolated DNA
  • Peripheral (whole) blood
Who can order: Help
  • Licensed Physician
Test Order Code: Help
MMP
View other test codes
CPT codes: Help
**AMA CPT codes notice

Copyright: 2023 American Medical Association. All rights reserved.

Lab contact: Help
Farid Chehab, PhD, MB(ASCP), Lab Director
farid.chehab@ucsf.edu
415-476-0310
Erik Samayoa, CLS, Laboratory Supervisor
Erik.Samayoa@ucsf.edu
415-514-8488
Contact Policy: Help
Laboratory can only accept contact from health care providers. Patients/families are encouraged to discuss genetic testing options with their health care provider.
How to Order: Help
Order URL
Informed consent required: Help
Decline to answer
Pre-test genetic counseling required: Help
Decline to answer
Post-test genetic counseling required: Help
Decline to answer
Recommended fields not provided:
Test strategy, Test development
Conditions Help
Total conditions: 1
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 52
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Methodology
Total methods: 1
Method Category Help
Test method Help
Instrument
Mutation scanning of select exons
Next-Generation (NGS)/Massively parallel sequencing (MPS)
Illumina MiSeq
Clinical Information
Test purpose: Help
Diagnosis; Drug Response; Monitoring; Prognostic; Therapeutic management
Target population: Help
Acute myeloid leukemia, myeodysplastic syndromes, primary myelifibrosis
Variant Interpretation:
What is the protocol for interpreting a variation as a VUS? Help
Unlisted or low population frequency in GnomAD, and absent from clinical databases

Are family members with defined clinical status recruited to assess significance of VUS without charge? Help
No.

Will the lab re-contact the ordering physician if variant interpretation changes? Help
Yes. The ordering physician will be contacted for issues on interpretation, ordering of follow-up tests or for patient clinical information.
Recommended fields not provided:
Clinical validity, Clinical utility, Is research allowed on the sample after clinical testing is complete?, Sample negative report, Sample positive report
Technical Information
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
Analytical sensitivity 1% Variant Allele Frequency (VAF)
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
Yes

Method used for proficiency testing: Help
Formal PT program

PT Provider: Help
College of American Pathologists, CAP

Description of PT method: Help
Next Generation Sequencing
VUS:
Laboratory's policy on reporting novel variations Help
Unlisted or low population frequency in GnomAD, and absent from clinical databases
Recommended fields not provided:
Test Confirmation, Assay limitations, Description of internal test validation method, Citations for Analytical validity, Major CAP category, CAP category, CAP test list
Regulatory Approval
FDA Review: Help
Not provided
Additional Information

IMPORTANT NOTE: NIH does not independently verify information submitted to GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.