ClinVar Miner

Submissions for variant NM_004958.4(MTOR):c.4449C>G (p.Cys1483Trp)

dbSNP: rs1057519913
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000440639 SCV000506725 likely pathogenic Glioblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000421869 SCV000506726 likely pathogenic Breast neoplasm 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000432577 SCV000506727 likely pathogenic Papillary renal cell carcinoma type 1 2016-05-31 no assertion criteria provided literature only

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