ClinVar Miner

Submissions for variant NM_182919.4(TICAM1):c.696C>T (p.Asp232=)

gnomAD frequency: 0.00018  dbSNP: rs574449966
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 RCV001088836 SCV000652810 likely benign Herpes simplex encephalitis, susceptibility to, 4 2023-11-28 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000536302 SCV001151596 likely benign not provided 2022-09-01 criteria provided, single submitter clinical testing TICAM1: BP4, BP7

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