ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.1401C>T (p.Asp467=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV004589078 SCV005085264 benign Familial cancer of breast 2024-04-29 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.
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV004596619 SCV005090003 likely benign not specified 2024-07-31 criteria provided, single submitter clinical testing

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