ClinVar Miner

Submissions for variant NM_014363.6(SACS):c.477C>T (p.Tyr159=)

dbSNP: rs1870531490
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV001289172 SCV001476821 uncertain significance not provided 2020-04-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002070096 SCV002360829 likely benign Spastic paraplegia 2023-07-28 criteria provided, single submitter clinical testing

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