ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.807G>T (p.Gly269=)

dbSNP: rs1399656182
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000776637 SCV000912257 likely benign Hereditary cancer-predisposing syndrome 2017-10-08 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004792451 SCV005403583 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.

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