ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.681A>G (p.Thr227=)

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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. RCV004787609 SCV005405315 benign Hereditary diffuse gastric adenocarcinoma 2024-09-13 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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