ClinVar Miner

Submissions for variant NM_005886.3(KATNB1):c.930G>C (p.Thr310=)

dbSNP: rs147460464
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000909179 SCV001053974 benign not provided 2023-09-27 criteria provided, single submitter clinical testing
GeneDx RCV000909179 SCV001778134 likely benign not provided 2021-02-23 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001818815 SCV002070323 likely benign not specified 2019-07-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000909179 SCV005218511 likely benign not provided criteria provided, single submitter not provided

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