ClinVar Miner

Submissions for variant NM_006019.4(TCIRG1):c.528C>A (p.Pro176=)

gnomAD frequency: 0.00135  dbSNP: rs538805960
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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) RCV000277239 SCV000335802 benign not specified 2015-10-08 criteria provided, single submitter clinical testing
Invitae RCV000968221 SCV001115660 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003955452 SCV004773165 likely benign TCIRG1-related disorder 2024-01-16 criteria provided, single submitter 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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