ClinVar Miner

Submissions for variant NM_004327.4(BCR):c.2699A>G (p.Asn900Ser)

gnomAD frequency: 0.00002  dbSNP: rs752530462
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Molecular Diagnostics and Monitoring of CML and Ph+ Leukemias, Institute of Hematology and Blood Transfusion RCV000171137 SCV000187708 not provided Chronic myelogenous leukemia, BCR-ABL1 positive no assertion provided not provided

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