ClinVar Miner

Submissions for variant NM_001664.4(RHOA):c.13C>T (p.Arg5Trp) (rs1057519952)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000420653 SCV000507301 likely pathogenic Carcinoma of esophagus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000430517 SCV000507302 likely pathogenic Breast neoplasm 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000441218 SCV000507303 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000423113 SCV000507304 likely pathogenic Non-Hodgkin lymphoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000430318 SCV000507305 likely pathogenic Adenocarcinoma of stomach 2016-05-31 no assertion criteria provided literature only

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