ClinVar Miner

Submissions for variant NM_000038.6(APC):c.3555A>C (p.Thr1185=)

dbSNP: rs786201125
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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 RCV001179719 SCV001344446 likely benign Hereditary cancer-predisposing syndrome 2019-10-02 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004564595 SCV004930682 benign Familial adenomatous polyposis 1 2024-03-21 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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