ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.918T>C (p.Cys306=)

dbSNP: rs761264502
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 RCV001481003 SCV001685337 likely benign NIK deficiency 2022-10-27 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003411903 SCV004140711 likely benign not provided 2022-12-01 criteria provided, single submitter clinical testing MAP3K14: BP4, BP7

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