ClinVar Miner

Submissions for variant NM_004656.4(BAP1):c.*444C>T

gnomAD frequency: 0.03611  dbSNP: rs123598
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000361941 SCV000445455 likely benign BAP1-related tumor predisposition syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001546080 SCV001765534 likely benign not provided 2019-06-15 criteria provided, single submitter clinical testing

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