ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.330del (p.Leu111fs)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Laboratory, Skane University Hospital Lund RCV004698183 SCV005198846 pathogenic not provided 2023-04-12 criteria provided, single submitter clinical testing
Clinical Genetics and Genomics, Karolinska University Hospital RCV004797649 SCV005419173 likely pathogenic TP53-related disorder 2024-10-01 no assertion criteria provided clinical testing

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