ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.792G>A (p.Gln264=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV004791995 SCV005406569 benign Hereditary diffuse gastric adenocarcinoma 2024-09-16 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.
Labcorp Genetics (formerly Invitae), Labcorp RCV004791995 SCV005828621 likely benign Hereditary diffuse gastric adenocarcinoma 2024-03-14 criteria provided, single submitter clinical testing

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