ClinVar Miner

Submissions for variant NM_152743.4(BRAT1):c.1867G>A (p.Gly623Ser)

gnomAD frequency: 0.01031  dbSNP: rs77015302
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000515026 SCV000609957 likely benign not provided 2017-08-31 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001084167 SCV000652243 benign Neonatal-onset encephalopathy with rigidity and seizures 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV000515026 SCV001900520 benign not provided 2019-07-24 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000515026 SCV005228321 likely benign not provided criteria provided, single submitter not provided

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