ClinVar Miner

Submissions for variant NM_001904.4(CTNNB1):c.98C>G (p.Ser33Cys) (rs121913400)

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Total submissions: 15
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000419399 SCV000505386 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000429684 SCV000505387 likely pathogenic Transitional cell carcinoma of the bladder 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000441671 SCV000505388 likely pathogenic Neoplasm of brain 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000420513 SCV000505389 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000430769 SCV000505390 likely pathogenic Hepatocellular carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000441027 SCV000505391 likely pathogenic Malignant neoplasm of body of uterus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000421624 SCV000505392 likely pathogenic Medulloblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000431875 SCV000505393 likely pathogenic Carcinoma of esophagus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000438635 SCV000505394 likely pathogenic Ovarian Neoplasms 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000421237 SCV000505395 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000432807 SCV000505396 likely pathogenic Neoplasm of the parathyroid gland 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000444407 SCV000505397 likely pathogenic Adenocarcinoma of stomach 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000425323 SCV000505398 likely pathogenic Pancreatic adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000432570 SCV000505399 likely pathogenic Adenocarcinoma of prostate 2016-05-31 no assertion criteria provided literature only
Donald Williams Parsons Laboratory,Baylor College of Medicine RCV000421624 SCV000599910 other Medulloblastoma 2016-05-01 no assertion criteria provided clinical testing

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