ClinVar Miner

Submissions for variant NM_182919.4(TICAM1):c.57C>T (p.Gly19=)

gnomAD frequency: 0.00041  dbSNP: rs113493978
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000957842 SCV001104660 likely benign Herpes simplex encephalitis, susceptibility to, 4 2024-01-24 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003424496 SCV004146321 likely benign not provided 2023-03-01 criteria provided, single submitter clinical testing TICAM1: BP4, BP7
Breakthrough Genomics, Breakthrough Genomics RCV003424496 SCV005206509 likely benign not provided criteria provided, single submitter not provided

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