ClinVar Miner

Submissions for variant NM_024675.4(PALB2):c.3004_3008del (p.Glu1002fs)

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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. RCV003140327 SCV003806537 pathogenic Familial cancer of breast 2023-01-12 criteria provided, single submitter clinical testing This variant is considered pathogenic. This variant creates a frameshift predicted to result in premature protein truncation.
Baylor Genetics RCV003140327 SCV004202122 likely pathogenic Familial cancer of breast 2023-08-20 criteria provided, single submitter clinical testing

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