ClinVar Miner

Submissions for variant NM_013432.5(TONSL):c.1149C>T (p.Ser383=)

gnomAD frequency: 0.00082  dbSNP: rs150235596
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001514176 SCV001721957 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001514176 SCV005270282 benign not provided criteria provided, single submitter not provided

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