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Genetic Labs

Houston, Texas

Genetic Laboratory
Baylor Genetics Laboratories
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Medical Genetics Test Details

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The American Medical Association (AMA) Current Procedural Terminology (CPT) codes and Healthcare Common Procedure Coding System (HCPCS) codes listed, are provided for informational purposes only. The codes reflect our interpretation of CPT/HCPCS coding requirements based upon AMA guidelines published annually. CPT/HCPCS codes are provided only as guidance to assist clients with billing. Baylor Genetics strongly recommends that clients confirm CPT/HCPCS codes with their Medicare Administrative Contractor (MAC) or other payer being billed, as requirements may differ. CPT coding is the sole responsibility of the billing party. Baylor Genetics assumes no responsibility for billing errors due to reliance on the CPT codes listed. Please direct any questions regarding CPT coding to the payer being billed.
SDHC - Related Disorders tests available.

Mitochondrial Respiratory Chain Complex II Deficiency | SDHC-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome | Paragangliomas 3 | PHEO and PGL Associated Syndrome Panel | PHEO/PGL Syndrome | PGL/PCC | PHEO and PGL Associated Syndrome | Hereditary Paraganglioma-Pheochromocytoma Syndromes

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Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing
Sequence Analysis SDHC Sequence Analysis
Test Code: 3190
SDHC Sequence Analysis
Test Code: 3191

This test can only be performed if there is a previously identified familial mutation.
SDHC Sequence Analysis
Test Code: 3191

This test can only be performed if there is a previously identified familial mutation.


SDHC Sequence Analysis
Test Information: Confirmation of Clinical Diagnosis
Test Details
Test Code: 3190
Special Notes: If the mutation to be tested in this individual is one previously identified in an affected family member, please order test code #3191. Please see detailed requirements under this test code.

SDHC is part of the PHEO and PGL Syndrome Panel test code #3600, which also includes SDHB and SDHD.

* Previously listed as test code 93190.
Technical Information
Methodology: Sequence analysis is performed in both forward and reverse directions
Gene Name: SDHC
Protein Name: Succinate dehydrogenase cytochrome b560 subunit
Test Type: Sequence Analysis
Sample & Shipping Information
Test Requisition: Mitochondrial
Specimen Type: Blood
Requirements: Draw blood in an EDTA (purple-top) tube(s) and send 3-5 cc (Adults/Children) and 3 cc (Infant<2yrs).
Shipping Conditions: Ship at room temperature in an insulated container by overnight courier. Do not heat or freeze.

Specimen Type: Saliva
Requirements: Collected with Oragene DNA Self-Collection Kit (provided by MGL with instruction).
Shipping Conditions: Ship at room temperature in an insulated container by overnight courier. Do not heat or freeze.

Turn Around Time: 28 days
Billing Information
List Price: *For Insurance or Institutional Prices, please call.
CPT Codes: 81405x1


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