ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.1464A>G (p.Pro488=)

gnomAD frequency: 0.00001  dbSNP: rs777565576
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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 RCV001501429 SCV001706241 likely benign NIK deficiency 2023-04-24 criteria provided, single submitter clinical testing

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