ClinVar Miner

Submissions for variant NM_006013.4(RPL10):c.291C>T (p.Ile97=) (rs138325578)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000153857 SCV000203440 uncertain significance not provided 2014-04-11 criteria provided, single submitter clinical testing
Ambry Genetics RCV000718360 SCV000849222 likely benign History of neurodevelopmental disorder 2017-04-04 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign;In silico models in agreement (benign)

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