ClinVar Miner

Submissions for variant NM_005732.4(RAD50):c.1275A>G (p.Lys425=) (rs769385714)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000859042 SCV000628143 likely benign not provided 2018-09-22 criteria provided, single submitter clinical testing
Ambry Genetics RCV000527089 SCV000671830 likely benign Hereditary cancer-predisposing syndrome 2016-12-07 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign

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