ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1742A>G (p.Asn581Ser) (rs121913370)

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Total submissions: 9
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000154399 SCV000204066 likely pathogenic Non-small cell lung cancer 2013-07-19 criteria provided, single submitter clinical testing
Database of Curated Mutations (DoCM) RCV000430462 SCV000505032 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000440277 SCV000505033 likely pathogenic Papillary renal cell carcinoma, sporadic 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000419529 SCV000505034 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000429356 SCV000505035 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000440055 SCV000505036 likely pathogenic Chronic myelogenous leukemia 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000421956 SCV000505037 likely pathogenic Cutaneous melanoma 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000432607 SCV000505038 likely pathogenic Ovarian Serous Cystadenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000438933 SCV000505039 likely pathogenic Multiple myeloma 2016-05-31 no assertion criteria provided literature only

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