ClinVar Miner

Submissions for variant NM_000244.3(MEN1):c.1095C>T (p.Ile365=) (rs147331514)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000203990 SCV000259317 likely benign not provided 2019-03-04 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000506264 SCV000604205 likely benign not specified 2016-09-12 criteria provided, single submitter clinical testing
Ambry Genetics RCV000574517 SCV000664496 likely benign Hereditary cancer-predisposing syndrome 2015-12-04 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign

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