ClinVar Miner

Submissions for variant NM_182919.4(TICAM1):c.479C>T (p.Ser160Phe)

gnomAD frequency: 0.00235  dbSNP: rs145148929
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000547869 SCV000652808 likely benign Herpes simplex encephalitis, susceptibility to, 4 2024-01-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003884631 SCV004701355 likely benign not provided 2023-12-01 criteria provided, single submitter clinical testing TICAM1: BP4, BS2

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