ClinVar Miner

Submissions for variant NM_002467.6(MYC):c.173C>T (p.Pro58Leu) (rs1057519918)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000428982 SCV000506758 likely pathogenic Carcinoma of esophagus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000436178 SCV000506759 likely pathogenic Neuroblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000418915 SCV000506760 likely pathogenic Non-Hodgkin lymphoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000427867 SCV000506761 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000438593 SCV000506762 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only

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