skip to content »

Genetic Labs

Houston, Texas

Genetic Laboratory
Baylor Genetics Laboratories
not shown on screen

Medical Genetics Test Details

View Custom Req   |    Tests in Custom Req: 0
Search Tests: (Search by disease, test name, gene name, test code, or keyword. Return to test index.)

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.
SURF1 - Related Disorders tests available.

Complex IV (COX) Deficiency | Leigh Syndrome Due to Cytochrome c Oxidase Deficiency | Leigh Disease | Leigh Syndrome (nuclear DNA mutation) | Mitochondrial Respiratory Chain Complex IV Deficiency (nuclear genes) | COX Deficiency (nuclear genes) | Cytochrome c Oxidase Deficiency

(Click the blue dot to view test details. Red dot = current test.)
Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing
Deletion/Duplication Analysis SURF1 Deletion/Duplication Analysis
Test Code: 3088
Sequence & Deletion/Duplication Analysis SURF1 Comprehensive - Sequence & Deletion/Duplication Analysis
Test Code: 3089
Sequence Analysis SURF1 Sequence Analysis
Test Code: 3085
SURF1 Sequence Analysis
Test Code: 3086

This test can only be performed if there is a previously identified familial mutation.
SURF1 Sequence Analysis
Test Code: 3087

We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to submitting any samples. Please call 1-800-411-4363.

SURF1 Sequence Analysis
Test Information: Confirmation of Clinical Diagnosis
Test Details
Test Code: 3085
Special Notes: If the mutation to be tested in this individual is one previously identified in an affected family member, please order test (#3086). Please see detailed requirements under this test code.

Technical Information
Methodology: Sequence analysis is performed in both forward and reverse directions
Gene Name: SURF1
Protein Name: Surfeit locus protein 1
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

Return to test index