ClinVar Miner

Submissions for variant NM_003954.5(MAP3K14):c.764C>T (p.Thr255Met)

gnomAD frequency: 0.00006  dbSNP: rs11574820
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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 RCV001422903 SCV001625463 likely benign NIK deficiency 2022-08-06 criteria provided, single submitter clinical testing

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