ClinVar Miner

Submissions for variant NM_000222.2(KIT):c.910A>G (p.Thr304Ala) (rs202052259)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000034511 SCV000560704 likely benign not provided 2019-03-04 criteria provided, single submitter clinical testing
Ambry Genetics RCV001018858 SCV001180145 uncertain significance Hereditary cancer-predisposing syndrome 2019-05-21 criteria provided, single submitter clinical testing Insufficient evidence
Biesecker Lab/Clinical Genomics Section,National Institutes of Health RCV000034511 SCV000043277 variant of unknown significance not provided 2012-07-13 no assertion criteria provided research Converted during submission to Uncertain significance.

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