ClinVar Miner

Submissions for variant NM_000546.5(TP53):c.147T>C (p.Asp49=) (rs786201148)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000162767 SCV000213244 likely benign Hereditary cancer-predisposing syndrome 2015-04-07 criteria provided, single submitter clinical testing
Color RCV000162767 SCV000686723 likely benign Hereditary cancer-predisposing syndrome 2017-01-17 criteria provided, single submitter clinical testing
Invitae RCV000633412 SCV000754634 likely benign Li-Fraumeni syndrome 2017-12-15 criteria provided, single submitter clinical testing

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