ClinVar Miner

Submissions for variant NM_001039141.3(TRIOBP):c.6899T>C (p.Val2300Ala)

gnomAD frequency: 0.00748  dbSNP: rs61737841
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000036834 SCV000060489 benign not specified 2012-04-30 criteria provided, single submitter clinical testing Val2300Ala in Exon 22 of TRIOBP: This variant is not expected to have clinical s ignificance because it has been identified in 1.8% (60/3292) of African American chromosomes from a broad population by the NHLBI Exome Sequencing Project (http ://evs.gs.washington.edu/EVS; dbSNP rs61737841).
PreventionGenetics, part of Exact Sciences RCV000036834 SCV000306119 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV000840104 SCV000982020 benign not provided 2019-05-16 criteria provided, single submitter clinical testing
Invitae RCV000840104 SCV001031890 benign not provided 2024-01-18 criteria provided, single submitter clinical testing

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