ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.7889T>G (p.Leu2630Ter)

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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 RCV003466665 SCV004212178 likely pathogenic Familial cancer of breast 2022-11-02 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV003466665 SCV004932248 pathogenic Familial cancer of breast 2024-02-01 criteria provided, single submitter clinical testing This variant is considered pathogenic. This variant creates a termination codon and is predicted to result in premature protein truncation.

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