ClinVar Miner

Submissions for variant NM_004281.3(BAG3):c.114C>T (p.Phe38=) (rs727504929)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000156322 SCV000206040 likely benign not specified 2014-01-21 criteria provided, single submitter clinical testing Phe38Phe in exon 1 of BAG3: This variant is not expected to have clinical signif icance because it is not located within the splice consensus sequence. Phe38Phe in exon 1 of BAG3 (allele frequency = n/a)

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