ClinVar Miner

Submissions for variant NM_001664.4(RHOA):c.14G>T (p.Arg5Leu)

dbSNP: rs1057519953
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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) RCV000432532 SCV000507311 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000444013 SCV000507312 likely pathogenic Breast neoplasm 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000425080 SCV000507313 likely pathogenic Non-Hodgkin lymphoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000431457 SCV000507314 likely pathogenic Carcinoma of esophagus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000443944 SCV000507315 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only

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