ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1790T>A (p.Leu597Gln) (rs121913366)

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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) RCV000431444 SCV000504273 pathogenic Cutaneous melanoma 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000443326 SCV000504274 likely pathogenic Multiple myeloma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000427485 SCV000504275 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000437736 SCV000504276 likely pathogenic Adenocarcinoma of prostate 2016-05-31 no assertion criteria provided literature only

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