ClinVar Miner

Submissions for variant NM_004281.3(BAG3):c.1422C>T (p.Ala474=) (rs727505000)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000156421 SCV000206139 likely benign not specified 2014-03-19 criteria provided, single submitter clinical testing Ala474Ala in exon 4 of BAG3: This variant is not expected to have clinical signi ficance because it does not alter an amino acid residue and is not located withi n the splice consensus sequence.
Invitae RCV000964700 SCV001111933 likely benign not provided 2018-12-28 criteria provided, single submitter clinical testing

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