ClinVar Miner

Submissions for variant NM_004958.4(MTOR):c.7498A>T (p.Ile2500Phe)

dbSNP: rs1057519916
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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) RCV000427238 SCV000506735 likely pathogenic Papillary renal cell carcinoma type 1 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000437898 SCV000506736 likely pathogenic Breast neoplasm 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000420686 SCV000506737 likely pathogenic Malignant neoplasm of body of uterus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000429674 SCV000506738 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only

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