ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.1098A>G (p.Arg366=)

gnomAD frequency: 0.00001  dbSNP: rs772065458
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 RCV001047922 SCV001211906 likely benign NIK deficiency 2024-01-29 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003425894 SCV004140709 likely benign not provided 2023-02-01 criteria provided, single submitter clinical testing MAP3K14: BP4, BP7

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