ClinVar Miner

Submissions for variant NM_000038.6(APC):c.3036T>A (p.Asn1012Lys)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics and NGS Laboratory, Hospital Fundacion Valle Del Lili RCV003484463 SCV004228994 likely pathogenic Familial adenomatous polyposis 1; Colorectal cancer 2024-01-06 criteria provided, single submitter clinical testing

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