ClinVar Miner

Submissions for variant NM_000038.6(APC):c.2388T>C (p.Tyr796=)

dbSNP: rs1554084124
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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 RCV000582496 SCV000686890 likely benign Hereditary cancer-predisposing syndrome 2017-08-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV004562571 SCV003519862 likely benign Familial adenomatous polyposis 1 2022-04-02 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004562571 SCV004933281 benign Familial adenomatous polyposis 1 2024-03-12 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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