ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1893A>T (p.Thr631=)

dbSNP: rs786201452
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000216798 SCV000273713 likely benign Hereditary cancer-predisposing syndrome 2015-01-26 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Labcorp Genetics (formerly Invitae), Labcorp RCV000546644 SCV000637757 likely benign Hereditary diffuse gastric adenocarcinoma 2023-09-25 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000216798 SCV000689491 likely benign Hereditary cancer-predisposing syndrome 2017-07-13 criteria provided, single submitter clinical testing

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