ClinVar Miner

Submissions for variant NM_005444.3(CNOT9):c.259T>C (p.Ser87Pro)

dbSNP: rs1057519956
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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) RCV000422236 SCV000507327 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000431636 SCV000507328 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000438382 SCV000507329 likely pathogenic Prostate adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000421602 SCV000507330 likely pathogenic Transitional cell carcinoma of the bladder 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000431838 SCV000507331 likely pathogenic Hepatocellular carcinoma 2016-05-31 no assertion criteria provided literature only

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