ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.2101C>T (p.Leu701Phe)

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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 RCV003466572 SCV004209401 uncertain significance Familial cancer of breast 2023-09-23 criteria provided, single submitter clinical testing
Department of Human Genetics, Hannover Medical School RCV003466572 SCV005324762 uncertain significance Familial cancer of breast 2024-09-17 criteria provided, single submitter clinical testing

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