ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.1660G>T (p.Asp554Tyr)

gnomAD frequency: 0.00016  dbSNP: rs770924893
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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 RCV001490037 SCV001694593 likely benign NIK deficiency 2023-10-22 criteria provided, single submitter clinical testing

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