ClinVar Miner

Submissions for variant NM_000038.6(APC):c.5632A>C (p.Lys1878Gln)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003459853 SCV004191428 uncertain significance Familial adenomatous polyposis 1 2023-09-07 criteria provided, single submitter clinical testing
Zotz-Klimas Genetics Lab, MVZ Zotz Klimas RCV003459853 SCV004099317 uncertain significance Familial adenomatous polyposis 1 2023-10-30 no assertion criteria provided clinical testing

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