ClinVar Miner

Submissions for variant NM_001375524.1(TRRAP):c.10512G>A (p.Thr3504=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002938368 SCV003266464 benign not provided 2023-12-07 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002938368 SCV004162598 likely benign not provided 2022-11-01 criteria provided, single submitter clinical testing TRRAP: BP4, BP7

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