ClinVar Miner

Submissions for variant NM_001904.4(CTNNB1):c.110C>G (p.Ser37Cys)

dbSNP: rs121913403
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Total submissions: 14
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000019141 SCV000039429 pathogenic Neoplasm of ovary 1999-05-01 no assertion criteria provided literature only
OMIM RCV000030945 SCV000039438 pathogenic Pilomatrixoma 1999-04-01 no assertion criteria provided literature only
Richard Lifton Laboratory, Yale University School of Medicine RCV000087195 SCV000120057 probable-pathogenic not provided flagged submission not provided Converted during submission to Likely pathogenic.
Richard Lifton Laboratory, Yale University School of Medicine RCV000087195 SCV000155160 probable-pathogenic not provided no assertion criteria provided not provided Converted during submission to Likely pathogenic.
Database of Curated Mutations (DoCM) RCV000441696 SCV000505451 likely pathogenic Prostate adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000423597 SCV000505452 likely pathogenic Hepatocellular carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000430788 SCV000505453 likely pathogenic Neoplasm of uterine cervix 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000438791 SCV000505454 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000421574 SCV000505455 likely pathogenic Malignant neoplasm of body of uterus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000431366 SCV000505456 likely pathogenic Medulloblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000445258 SCV000505457 likely pathogenic Transitional cell carcinoma of the bladder 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000422240 SCV000505458 likely pathogenic Carcinoma of esophagus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000432924 SCV000505459 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000019141 SCV000505460 likely pathogenic Neoplasm of ovary 2015-07-14 no assertion criteria provided literature only

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