ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1790T>G (p.Leu597Arg) (rs121913366)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000015002 SCV000035258 pathogenic Lung adenocarcinoma 2003-08-15 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000439504 SCV000504268 pathogenic Cutaneous melanoma 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000421775 SCV000504269 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000432024 SCV000504270 likely pathogenic Multiple myeloma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000444137 SCV000504271 pathogenic Ovarian Neoplasms 2014-10-02 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000421201 SCV000504272 likely pathogenic Adenocarcinoma of prostate 2016-05-31 no assertion criteria provided literature only

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