ClinVar Miner

Submissions for variant NM_024529.4(CDC73):c.33C>T (p.Tyr11=) (rs150951102)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000425634 SCV000530378 likely benign not specified 2017-06-26 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Illumina Clinical Services Laboratory,Illumina RCV000267832 SCV000352119 likely benign Hyperparathyroidism 2 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000232276 SCV000352120 likely benign Parathyroid carcinoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000372976 SCV000352121 likely benign Isolated Hyperparathyroidism 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000232276 SCV000290767 benign Parathyroid carcinoma 2018-01-18 criteria provided, single submitter clinical testing

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