ClinVar Miner

Submissions for variant NM_001039141.3(TRIOBP):c.3774C>T (p.Pro1258=)

gnomAD frequency: 0.00020  dbSNP: rs377749969
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000397770 SCV000339958 uncertain significance not provided 2017-01-19 criteria provided, single submitter clinical testing
GeneDx RCV000397770 SCV001805305 likely benign not provided 2020-08-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000397770 SCV003289737 likely benign not provided 2022-09-01 criteria provided, single submitter clinical testing

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