ClinVar Miner

Submissions for variant NM_016734.3(PAX5):c.1074del (p.Ser357_Trp358insTer)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Diagnostics Laboratory, National Institute of Medical Genomics RCV003444118 SCV004036041 likely pathogenic Acute lymphoid leukemia 2023-09-23 criteria provided, single submitter clinical testing

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