ClinVar Miner

Submissions for variant NM_001654.5(ARAF):c.641C>G (p.Ser214Cys) (rs1057519786)

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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) RCV000427514 SCV000505155 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000436910 SCV000505156 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000419218 SCV000505157 not provided Non-small cell lung cancer 2016-03-10 no assertion provided literature only
Database of Curated Mutations (DoCM) RCV000430187 SCV000505158 likely pathogenic Papillary renal cell carcinoma, sporadic 2016-05-31 no assertion criteria provided literature only

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