ClinVar Miner

Submissions for variant NM_000546.5(TP53):c.782+17C>T (rs17880172)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000578079 SCV000686772 likely benign Hereditary cancer-predisposing syndrome 2015-07-21 criteria provided, single submitter clinical testing
GeneDx RCV000125576 SCV000169028 benign not specified 2014-01-03 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.
Institute for Biomarker Research,Medical Diagnostic Laboratories, L.L.C. RCV000578079 SCV000679748 likely benign Hereditary cancer-predisposing syndrome 2017-07-12 criteria provided, single submitter clinical testing
PreventionGenetics RCV000125576 SCV000806248 benign not specified 2017-06-07 criteria provided, single submitter clinical testing

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