ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.2715C>T (p.Asp905=)

gnomAD frequency: 0.00001  dbSNP: rs371657957
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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 RCV002152462 SCV002420683 likely benign NIK deficiency 2024-01-02 criteria provided, single submitter clinical testing

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