ClinVar Miner

Submissions for variant NM_000481.3(AMT):c.898A>G (p.Met300Val) (rs144971200)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000224316 SCV000281318 likely benign not provided 2015-10-28 criteria provided, single submitter clinical testing Converted during submission to Likely benign.
Illumina Clinical Services Laboratory,Illumina RCV000263419 SCV000445373 uncertain significance Non-ketotic hyperglycinemia 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000224316 SCV000636430 benign not provided 2019-03-05 criteria provided, single submitter clinical testing

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