ClinVar Miner

Submissions for variant NM_001904.4(CTNNB1):c.122C>T (p.Thr41Ile)

dbSNP: rs121913413
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Total submissions: 9
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000019152 SCV000039440 pathogenic Pilomatrixoma 1999-04-01 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000442963 SCV000506041 likely pathogenic Hepatocellular carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000422057 SCV000506042 likely pathogenic Prostate adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000432291 SCV000506043 likely pathogenic Neoplasm of the large intestine 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000443038 SCV000506044 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000426659 SCV000506045 likely pathogenic Malignant neoplasm of body of uterus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000436836 SCV000506046 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000442251 SCV000506047 likely pathogenic Adrenal cortex carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000427656 SCV000506048 likely pathogenic Pancreatic adenocarcinoma 2016-05-31 no assertion criteria provided literature only

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