ClinVar Miner

Submissions for variant NM_000546.5(TP53):c.769C>T (p.Leu257=) (rs779761818)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000219727 SCV000278211 likely benign Hereditary cancer-predisposing syndrome 2015-09-06 criteria provided, single submitter clinical testing
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000583437 SCV000692071 likely benign not specified no assertion criteria provided clinical testing

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