ClinVar Miner

Submissions for variant NM_001904.4(CTNNB1):c.95A>G (p.Asp32Gly)

dbSNP: rs121913396
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Total submissions: 12
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000019140 SCV000039428 pathogenic Pilomatrixoma 1999-04-01 no assertion criteria provided literature only
Richard Lifton Laboratory, Yale University School of Medicine RCV000087199 SCV000120061 probable-pathogenic not provided flagged submission not provided Converted during submission to Likely pathogenic.
Richard Lifton Laboratory, Yale University School of Medicine RCV000087199 SCV000155164 probable-pathogenic not provided no assertion criteria provided not provided Converted during submission to Likely pathogenic.
Database of Curated Mutations (DoCM) RCV000433199 SCV000505356 likely pathogenic Prostate adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000443883 SCV000505357 likely pathogenic Melanoma 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000427454 SCV000505358 likely pathogenic Neoplasm of uterine cervix 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000437703 SCV000505359 likely pathogenic Hepatocellular carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000443060 SCV000505360 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000425010 SCV000505361 likely pathogenic Transitional cell carcinoma of the bladder 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000435333 SCV000505362 likely pathogenic Malignant neoplasm of body of uterus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000417687 SCV000505363 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000427896 SCV000505364 likely pathogenic Medulloblastoma 2016-05-31 no assertion criteria provided literature only

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