ClinVar Miner

List of variants reported as benign for NIK deficiency

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP
NM_003954.5(MAP3K14):c.132C>T (p.Ala44=) rs55740287
NM_003954.5(MAP3K14):c.2020C>T (p.His674Tyr) rs11867907
NM_003954.5(MAP3K14):c.2434-10G>A rs34836788
NM_003954.5(MAP3K14):c.326+10G>A rs372339711
NM_003954.5(MAP3K14):c.419G>A (p.Ser140Asn) rs11574819
NM_003954.5(MAP3K14):c.521G>A (p.Cys174Tyr) rs184263319
NM_003954.5(MAP3K14):c.774C>G (p.Phe258Leu) rs148344770

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.