ClinVar Miner

Submissions for variant NM_001039141.3(TRIOBP):c.1263T>C (p.Asn421=)

dbSNP: rs566207993
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000730494 SCV000858236 likely benign not specified 2017-11-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002536446 SCV003294677 benign not provided 2023-10-05 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003928228 SCV004744963 likely benign TRIOBP-related disorder 2019-05-20 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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