ClinVar Miner

List of variants in gene NOG reported as pathogenic for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP
NM_005450.5(NOG):c.103C>T (p.Pro35Ser) rs28937580
NM_005450.5(NOG):c.328C>T (p.Gln110Ter) rs104894614
NM_005450.5(NOG):c.614G>A (p.Trp205Ter) rs1567745119
NM_005450.5(NOG):c.615G>C (p.Trp205Cys) rs104894615
NM_005450.5(NOG):c.649T>G (p.Trp217Gly) rs104894603
NM_005450.5(NOG):c.696C>G (p.Cys232Trp) rs387906844
NM_005450.6(NOG):c.64dup (p.Ala22fs) rs1597919829
NOG, 1-BP DEL
NOG, 1-BP INS, 252C

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.