ClinVar Miner

Submissions for variant NM_001904.4(CTNNB1):c.133T>G (p.Ser45Ala)

dbSNP: rs121913407
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000420592 SCV000505466 likely pathogenic Disease 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000427795 SCV000505467 likely pathogenic Neoplasm of brain 2015-07-14 no assertion criteria provided literature only

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