ClinVar Miner

Submissions for variant NM_000245.4(MET):c.3688T>C (p.Tyr1230His)

dbSNP: rs121913247
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000175410 SCV000226887 uncertain significance not provided 2014-09-22 criteria provided, single submitter clinical testing
Database of Curated Mutations (DoCM) RCV000417458 SCV000505011 likely pathogenic Renal carcinoma 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000431224 SCV000505012 likely pathogenic Carcinoma 2016-05-13 no assertion criteria provided literature only

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