GTR Home > Tests > Mitochondrial genome sequencing


Test order codeHelp: 81479

Test name


Mitochondrial genome sequencing

Purpose of the test


This is a clinical test intended for Help: Diagnosis, Mutation Confirmation



531 conditions tested. Click Indication tab for more information.

How to order


After obtaining the patient specimen and patient information, please ship us the specimen and accompanying information to 1920 NE Stucki Ave, Suite 150, Hillsboro, OR 97006 The patient information and test details can be provided one of two ways: 1. Via our online submission platform ( - once the details have been input into the system, print out the packing slip and ship with the specimen. 2. Fill out and print a physical test requisition form from our website to ship with the specimen. If you have any further questions, please call 503-227-3179 or email
Order URL Help:

Specimen source

Amniotic fluid
Bone marrow
Buccal swab
Buffy coat
Cell culture
Chorionic villi
Cord blood
Dried blood spot (DBS) card
Fetal blood
Fresh tissue
Frozen tissue
Isolated DNA
Peripheral (whole) blood
White blood cell prep


Molecular Genetics
CSequence analysis of the entire coding region
SNP Detection
  • Illumina HiSeqâ„¢2000 system

Summary of what is tested

339 genes and variants. Click Methodology tab for more information.


Clinical utility


Not provided

Clinical validity


Not provided

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the 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.

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