ClinVar Miner

Submissions for variant NM_003318.5(TTK):c.2089G>T (p.Asp697Tyr)

dbSNP: rs1057520011
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV002244866 SCV000510410 likely pathogenic Neoplasm of the pancreas 2016-05-13 no assertion criteria provided literature only

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