ClinVar Miner

Submissions for variant NM_005120.3(MED12):c.3670C>T (p.Leu1224Phe)

dbSNP: rs1057519912
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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) RCV000426762 SCV000506709 likely pathogenic Squamous cell lung carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000433808 SCV000506710 likely pathogenic Breast neoplasm 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000445331 SCV000506711 likely pathogenic Pancreatic adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000425461 SCV000506712 likely pathogenic Prostate adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000436162 SCV000506713 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only

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