Web: | mayocliniclabs.com |
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Email: | mcl@mayo.edu |
Telephone: | 800-533-1710 |
International: | +1 855-379-3115 |
Values are valid only on day of printing. |
Aiding in the prognostication and clinical management of lymphoplasmacytic lymphoma/Waldenstrom macroglobulinemia
This test detects gene variants within the C-terminal end of the CXCR4 gene that are commonly found in association with MYD88 L265P variants in cases of lymphoplasmacytic lymphoma/Waldenstrom macroglobulinemia (LPL/WM).
This test offers highly sensitive detection of the well-characterized hotspot variants c.1013C->G/A, p.S338X and routine Sanger sequencing for other variant in the C-terminus region. It is strongly recommended that this test be used in the context of the MYD88 / MYD88, L265P, Somatic Gene Mutation, DNA Allele-Specific PCR assay during evaluation of lymphoplasmacytic lymphoma/Waldenstrom macroglobulinemia (LPL/WM).
Mutation Detection in DNA using BNAClamp Sanger Sequencing Technology and Routine Sanger Sequencing
(BNAClamp is utilized pursuant to a license agreement with BNA Inc)