ClinVar Miner

Submissions for variant NM_001664.4(RHOA):c.118G>C (p.Glu40Gln)

dbSNP: rs1057519951
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000425897 SCV000507293 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000436482 SCV000507294 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000443212 SCV000507295 likely pathogenic Squamous cell carcinoma of the head and neck 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000425677 SCV000507296 likely pathogenic Breast neoplasm 2016-05-31 no assertion criteria provided literature only

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