ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1786G>A (p.Gly596Ser) (rs121913361)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000423119 SCV000505830 likely pathogenic Glioblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000433824 SCV000505831 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000442552 SCV000505832 likely pathogenic Transitional cell carcinoma of the bladder 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000422893 SCV000505833 likely pathogenic Multiple myeloma 2016-05-31 no assertion criteria provided literature only

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