ClinVar Miner

Submissions for variant NM_001039141.3(TRIOBP):c.5322+5281GGC[8]

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003433208 SCV004147866 likely benign not provided 2023-07-01 criteria provided, single submitter clinical testing TRIOBP: BP3, BS2
PreventionGenetics, part of Exact Sciences RCV004753684 SCV005354211 benign TRIOBP-related disorder 2024-05-13 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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