ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.2415T>C (p.Asp805=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002466173 SCV002760865 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004785729 SCV005402958 benign Hereditary diffuse gastric adenocarcinoma 2024-09-23 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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