ClinVar Miner

Submissions for variant NM_002834.5(PTPN11):c.1508G>T (p.Gly503Val)

dbSNP: rs397507546
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000430281 SCV000507259 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000440091 SCV000507260 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000419381 SCV000507261 likely pathogenic Squamous cell lung carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000429259 SCV000507262 likely pathogenic Multiple myeloma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000439943 SCV000507263 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only
Donald Williams Parsons Laboratory, Baylor College of Medicine RCV000505671 SCV000599951 other Embryonal rhabdomyosarcoma 2016-05-01 no assertion criteria provided clinical testing

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