ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1787G>A (p.Gly596Asp) (rs397507483)

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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) RCV000432706 SCV000505834 likely pathogenic Multiple myeloma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000442687 SCV000505835 likely pathogenic Transitional cell carcinoma of the bladder 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000425257 SCV000505836 likely pathogenic Glioblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000435960 SCV000505837 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only

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