ClinVar Miner

Submissions for variant NM_016292.3(TRAP1):c.933T>C (p.His311=)

gnomAD frequency: 0.00172  dbSNP: rs142413437
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000676242 SCV002495454 benign not provided 2024-10-28 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000676242 SCV004144948 likely benign not provided 2024-08-01 criteria provided, single submitter clinical testing TRAP1: BP4, BP7
Breakthrough Genomics, Breakthrough Genomics RCV000676242 SCV005295896 benign not provided criteria provided, single submitter not provided
Mayo Clinic Laboratories, Mayo Clinic RCV000676242 SCV000801996 likely benign not provided 2018-03-19 no assertion criteria provided clinical testing

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