ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.1131C>T (p.Asn377=)

gnomAD frequency: 0.00002  dbSNP: rs750776653
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000976498 SCV001124402 likely benign NIK deficiency 2023-12-18 criteria provided, single submitter clinical testing

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