ClinVar Miner

Submissions for variant NM_006087.4(TUBB4A):c.293G>A (p.Gly98Asp)

dbSNP: rs1555754185
Minimum review status: Collection method:
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000591466 SCV000704704 uncertain significance not provided 2016-12-20 criteria provided, single submitter clinical testing
Ambry Genetics RCV001266342 SCV001444516 likely pathogenic Inborn genetic diseases 2018-03-28 criteria provided, single submitter clinical testing

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