ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1406G>C (p.Gly469Ala) (rs121913355)

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Total submissions: 12
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000150210 SCV000197154 pathogenic Non-small cell lung cancer 2014-08-25 criteria provided, single submitter clinical testing
OMIM RCV000015005 SCV000035261 pathogenic Non-Hodgkin lymphoma 2003-11-17 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000440864 SCV000504325 pathogenic Lung cancer 2014-10-02 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000419278 SCV000504326 pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000430006 SCV000504327 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000439801 SCV000504328 likely pathogenic Transitional cell carcinoma of the bladder 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000422572 SCV000504329 likely pathogenic Squamous cell carcinoma of the skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000432393 SCV000504330 likely pathogenic Squamous cell lung carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000439564 SCV000504331 likely pathogenic Adenocarcinoma of prostate 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000421485 SCV000504332 likely pathogenic Neoplasm 2016-05-13 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000432193 SCV000504333 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000444131 SCV000504334 likely pathogenic Multiple myeloma 2016-05-31 no assertion criteria provided literature only

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