ClinVar Miner

Submissions for variant NM_001903.5(CTNNA1):c.1046C>A (p.Ser349Ter)

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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. RCV003455952 SCV004186877 pathogenic Hereditary diffuse gastric adenocarcinoma 2023-08-31 criteria provided, single submitter clinical testing This variant is considered pathogenic. This variant creates a termination codon and is predicted to result in premature protein truncation.

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