ClinVar Miner

Submissions for variant NM_001903.5(CTNNA1):c.163T>C (p.Ser55Pro)

dbSNP: rs1755329623
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Center, National Cancer Institute RCV002274836 SCV002559841 uncertain significance Colorectal cancer no assertion criteria provided case-control

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