ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1742A>C (p.Asn581Thr) (rs121913370)

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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000430791 SCV000505845 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000440655 SCV000505846 likely pathogenic Ovarian Serous Cystadenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000419907 SCV000505847 likely pathogenic Papillary renal cell carcinoma, sporadic 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000429764 SCV000505848 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000440423 SCV000505849 likely pathogenic Multiple myeloma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000422334 SCV000505850 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Department of Pathology and Laboratory Medicine,Sinai Health System RCV001355069 SCV001549837 uncertain significance not provided no assertion criteria provided clinical testing

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