ClinVar Miner

Submissions for variant NM_001904.4(CTNNB1):c.109T>C (p.Ser37Pro)

dbSNP: rs121913228
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Total submissions: 10
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000440535 SCV000505431 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000423296 SCV000505432 likely pathogenic Malignant neoplasm of body of uterus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000429643 SCV000505433 likely pathogenic Hepatocellular carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000440333 SCV000505434 likely pathogenic Medulloblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000423953 SCV000505435 likely pathogenic Neoplasm of stomach 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000434676 SCV000505436 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000444541 SCV000505437 likely pathogenic Carcinoma of esophagus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000423766 SCV000505438 likely pathogenic Transitional cell carcinoma of the bladder 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000431861 SCV000505439 likely pathogenic Prostate adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000443827 SCV000505440 likely pathogenic Neoplasm of uterine cervix 2016-05-31 no assertion criteria provided literature only

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