ClinVar Miner

Submissions for variant NM_000546.5(TP53):c.919+9G>A (rs772829199)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000774784 SCV000908780 likely benign Hereditary cancer-predisposing syndrome 2018-01-06 criteria provided, single submitter clinical testing
GeneDx RCV000433493 SCV000514943 likely benign not specified 2017-10-13 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.
Invitae RCV000472694 SCV000557360 likely benign Li-Fraumeni syndrome 2017-12-27 criteria provided, single submitter clinical testing

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