ClinVar Miner

List of variants in gene COQ8B studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_024876.4(COQ8B):c.1035+7T>C rs2246095 0.56103
NM_024876.4(COQ8B):c.521A>G (p.His174Arg) rs3865452 0.47243
NM_024876.4(COQ8B):c.768G>A (p.Ala256=) rs11538385 0.22464
NM_024876.4(COQ8B):c.9G>A (p.Leu3=) rs11673492 0.16347
NM_024876.4(COQ8B):c.1055C>G (p.Thr352Arg) rs36012476 0.03290
NM_024876.4(COQ8B):c.648C>T (p.Ala216=) rs4803357 0.02373
NM_024876.4(COQ8B):c.232C>T (p.Arg78Cys) rs11538384 0.02355
NM_024876.4(COQ8B):c.718-8C>G rs78137400 0.01807
NM_024876.4(COQ8B):c.1365T>C (p.Tyr455=) rs17851001 0.01362
NM_024876.4(COQ8B):c.1119C>T (p.Phe373=) rs56056214 0.01001
NM_024876.4(COQ8B):c.1578C>T (p.Asp526=) rs56276635 0.00974
NM_024876.4(COQ8B):c.*10T>C rs61742811 0.00969
NM_024876.4(COQ8B):c.381G>A (p.Gly127=) rs55895642 0.00488
NM_024876.4(COQ8B):c.1347C>T (p.Phe449=) rs142420160 0.00400
NM_024876.4(COQ8B):c.1305C>T (p.Ser435=) rs139130454 0.00358
NM_024876.4(COQ8B):c.501C>A (p.Phe167Leu) rs55793080 0.00267
NM_024876.4(COQ8B):c.663G>A (p.Gly221=) rs142414537 0.00185
NM_024876.4(COQ8B):c.1036-3C>G rs200061712 0.00182
NM_024876.4(COQ8B):c.344T>C (p.Met115Thr) rs148374624 0.00147
NM_024876.4(COQ8B):c.1035+13G>C rs202196406 0.00070
NM_024876.4(COQ8B):c.1125T>C (p.Tyr375=) rs78185540 0.00025
NM_024876.4(COQ8B):c.706G>A (p.Val236Met) rs146225943 0.00017
NM_024876.4(COQ8B):c.597C>T (p.Leu199=) rs186764121 0.00014
NM_024876.4(COQ8B):c.786G>A (p.Ala262=) rs201537185 0.00007
NM_024876.4(COQ8B):c.289+13T>C rs371151776 0.00004
NM_024876.4(COQ8B):c.490+17G>A rs751178358 0.00004
NM_024876.4(COQ8B):c.1128T>C (p.Asp376=) rs1361328591 0.00001
NM_024876.4(COQ8B):c.1297-5C>A rs1261602445 0.00001
NM_024876.4(COQ8B):c.491-18G>C rs372213778 0.00001
NM_024876.4(COQ8B):c.96C>T (p.His32=) rs755263013 0.00001
NM_024876.4(COQ8B):c.1035+7_1035+8inv
NM_024876.4(COQ8B):c.1080G>A (p.Glu360=) rs1555756422
NM_024876.4(COQ8B):c.1210-10G>A rs77801349
NM_024876.4(COQ8B):c.1297-13C>T rs774086810
NM_024876.4(COQ8B):c.663G>T (p.Gly221=) rs142414537

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.