ClinVar Miner

Submissions for variant NM_014780.5(CUL7):c.2754G>A (p.Thr918=)

dbSNP: rs138777262
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000730812 SCV000858576 uncertain significance not provided 2017-12-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000730812 SCV001044216 likely benign not provided 2025-01-21 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003994100 SCV004813056 likely benign not specified 2024-02-16 criteria provided, single submitter clinical testing

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