ClinVar Miner

Submissions for variant NM_001664.4(RHOA):c.125A>C (p.Tyr42Ser) (rs1057519954)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000427521 SCV000507319 likely pathogenic Adenocarcinoma of stomach 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000436909 SCV000507320 likely pathogenic Squamous cell carcinoma of the head and neck 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000419217 SCV000507321 likely pathogenic Non-Hodgkin lymphoma 2016-05-31 no assertion criteria provided literature only

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