ClinVar Miner

List of variants in gene MAP3K14 reported as likely benign for NIK deficiency

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
Download table as spreadsheet
NM_003954.5(MAP3K14):c.1009C>T (p.Leu337=) rs374376396
NM_003954.5(MAP3K14):c.1546G>A (p.Val516Ile) rs367938510
NM_003954.5(MAP3K14):c.1587C>T (p.His529=) rs562409633
NM_003954.5(MAP3K14):c.2290A>G (p.Thr764Ala) rs56302559
NM_003954.5(MAP3K14):c.2292C>T (p.Thr764=) rs746706058
NM_003954.5(MAP3K14):c.2820T>C (p.His940=) rs751517422
NM_003954.5(MAP3K14):c.555C>T (p.Leu185=) rs191629489
NM_003954.5(MAP3K14):c.764C>T (p.Thr255Met) rs11574820
NM_003954.5(MAP3K14):c.880A>C (p.Lys294Gln) rs113278485

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.