ClinVar Miner

Submissions for variant NM_001904.4(CTNNB1):c.101G>T (p.Gly34Val) (rs28931589)

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Total submissions: 12
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000019146 SCV000039434 pathogenic Hepatoblastoma 1999-01-15 no assertion criteria provided literature only
Science for Life laboratory, Karolinska Institutet RCV000149120 SCV000088762 unknown Malignant tumor of prostate no assertion criteria provided not provided Converted during submission to Uncertain significance.
Database of Curated Mutations (DoCM) RCV000427137 SCV000505421 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000437867 SCV000505422 likely pathogenic Adenocarcinoma of stomach 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000418024 SCV000505423 likely pathogenic Medulloblastoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000425225 SCV000505424 likely pathogenic Craniopharyngioma 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000435058 SCV000505425 likely pathogenic Hepatocellular carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000417805 SCV000505426 likely pathogenic Malignant neoplasm of body of uterus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000429363 SCV000505427 likely pathogenic Adrenocortical carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000436574 SCV000505428 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000418475 SCV000505429 likely pathogenic Squamous cell carcinoma of the head and neck 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000428985 SCV000505430 likely pathogenic Melanoma 2015-07-14 no assertion criteria provided literature only

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