ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.3307C>T (p.Arg1103Trp)

gnomAD frequency: 0.00849  dbSNP: rs61739385
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Total submissions: 3
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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 RCV000514526 SCV000610492 likely benign not provided 2017-04-19 criteria provided, single submitter clinical testing
Invitae RCV000514526 SCV001024885 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV000514526 SCV001915217 benign not provided 2021-05-12 criteria provided, single submitter clinical testing

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