ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.306C>T (p.Ile102=)

gnomAD frequency: 0.00001  dbSNP: rs759009271
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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 RCV001482987 SCV001687368 likely benign NIK deficiency 2019-06-28 criteria provided, single submitter clinical testing

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