ClinVar Miner

List of variants in gene NCF2 reported as not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
Download table as spreadsheet
NM_000433.3(NCF2):c.1105G>A (p.Gly369Arg) rs137854513
NM_000433.3(NCF2):c.125A>G (p.Asn42Ser) rs137854514
NM_000433.3(NCF2):c.130G>C (p.Gly44Arg) rs137854510
NM_000433.3(NCF2):c.130G>T (p.Gly44Cys) rs137854510
NM_000433.3(NCF2):c.230G>A (p.Arg77Gln) rs119103275
NM_000433.3(NCF2):c.233G>A (p.Gly78Glu) rs137854519
NM_000433.3(NCF2):c.235A>G (p.Met79Val) rs137854512
NM_000433.3(NCF2):c.279C>G (p.Asp93Glu) rs137854507
NM_000433.3(NCF2):c.305G>C (p.Arg102Pro) rs137854515
NM_000433.3(NCF2):c.323A>T (p.Asp108Val) rs137854509
NM_000433.3(NCF2):c.383C>T (p.Ala128Val) rs119103274
NM_000433.3(NCF2):c.409T>A (p.Trp137Arg) rs137854516
NM_000433.3(NCF2):c.419C>A (p.Ala140Asp) rs137854520
NM_000433.3(NCF2):c.505C>G (p.Gln169Glu) rs137854517
NM_000433.3(NCF2):c.551G>C (p.Arg184Pro) rs137854518
NM_000433.3(NCF2):c.605C>T (p.Ala202Val) rs137854508
NM_000433.3(NCF2):c.983G>A (p.Arg328Lys) rs137854511

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.