ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.1118C>T (p.Pro373Leu)

gnomAD frequency: 0.00348  dbSNP: rs34273213
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000194982 SCV000249314 likely benign not specified 2015-03-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000905467 SCV001050052 benign not provided 2024-01-26 criteria provided, single submitter clinical testing

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