ClinVar Miner

Submissions for variant NM_001904.4(CTNNB1):c.100G>C (p.Gly34Arg) (rs121913399)

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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) RCV000436663 SCV000505402 likely pathogenic Malignant neoplasm of body of uterus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000419419 SCV000505403 likely pathogenic Squamous cell carcinoma of the head and neck 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000427501 SCV000505404 likely pathogenic Pilomatrixoma 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000438184 SCV000505405 likely pathogenic Craniopharyngioma 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000420040 SCV000505406 likely pathogenic Hepatocellular carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000430713 SCV000505407 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000438776 SCV000505408 likely pathogenic Adrenocortical carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000418083 SCV000505409 likely pathogenic Adenocarcinoma of stomach 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000427907 SCV000505410 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000438599 SCV000505411 likely pathogenic Medulloblastoma 2016-05-31 no assertion criteria provided literature only

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