ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1397G>T (p.Gly466Val) (rs121913351)

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Total submissions: 10
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000015001 SCV000035257 pathogenic Lung adenocarcinoma 2003-08-15 no assertion criteria provided literature only
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000037916 SCV000061578 pathogenic Non-small cell lung cancer 2009-05-29 no assertion criteria provided clinical testing
Database of Curated Mutations (DoCM) RCV000436576 SCV000504345 pathogenic Lung cancer 2014-10-02 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000037916 SCV000504346 likely pathogenic Non-small cell lung cancer 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000429151 SCV000504347 pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000438953 SCV000504348 likely pathogenic Squamous cell lung carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000421693 SCV000504349 likely pathogenic Multiple myeloma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000015001 SCV000504350 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000438708 SCV000504351 likely pathogenic Squamous cell carcinoma of the head and neck 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000424032 SCV000504352 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only

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