ClinVar Miner

Submissions for variant NM_001903.5(CTNNA1):c.2008dup (p.Arg670fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV003450575 SCV004185932 likely pathogenic Hereditary diffuse gastric adenocarcinoma 2023-11-20 criteria provided, single submitter clinical testing This variant is considered likely pathogenic. This variant creates a frameshift predicted to result in premature protein truncation.

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