ClinVar Miner

Submissions for variant NM_001904.4(CTNNB1):c.101G>A (p.Gly34Glu) (rs28931589)

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Total submissions: 11
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000019149 SCV000039437 pathogenic Pilomatrixoma 1999-04-01 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000422250 SCV000505412 likely pathogenic Squamous cell carcinoma of the head and neck 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000432939 SCV000505413 likely pathogenic Adrenocortical carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000439589 SCV000505414 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000423249 SCV000505415 likely pathogenic Adenocarcinoma of stomach 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000433938 SCV000505416 likely pathogenic Malignant neoplasm of body of uterus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000443851 SCV000505417 likely pathogenic Hepatocellular carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000426491 SCV000505418 likely pathogenic Ovarian Neoplasms 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000434538 SCV000505419 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000443977 SCV000505420 likely pathogenic Medulloblastoma 2016-05-31 no assertion criteria provided literature only
Donald Williams Parsons Laboratory,Baylor College of Medicine RCV000443977 SCV000599908 other Medulloblastoma 2016-05-01 no assertion criteria provided clinical testing

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