ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.2580C>T (p.Asp860=)

dbSNP: rs2152144118
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001525980 SCV001736210 likely benign Hereditary cancer-predisposing syndrome 2020-10-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002070332 SCV002417969 likely benign Hereditary diffuse gastric adenocarcinoma 2021-02-20 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002070332 SCV005407098 benign Hereditary diffuse gastric adenocarcinoma 2024-09-24 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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