ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.414A>G (p.Glu138=)

dbSNP: rs1555515193
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000586851 SCV000698400 likely benign not specified 2019-08-28 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004788001 SCV005405442 benign Hereditary diffuse gastric adenocarcinoma 2024-09-12 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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