ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.15del (p.Asn6fs)

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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 RCV003466656 SCV004212128 likely pathogenic Familial cancer of breast 2023-01-04 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV003466656 SCV004933844 pathogenic Familial cancer of breast 2024-01-05 criteria provided, single submitter clinical testing This variant is considered pathogenic. This variant creates a frameshift predicted to result in premature protein truncation.

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