ClinVar Miner

List of variants in gene VAPB reported as benign for amyotrophic lateral sclerosis type 8

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 51
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004738.5(VAPB):c.*5250T>C rs6015274 0.49186
NM_004738.5(VAPB):c.315+35C>T rs2234487 0.43269
NM_004738.5(VAPB):c.*5298C>T rs6015275 0.22495
NM_004738.5(VAPB):c.*4271A>G rs4549163 0.15908
NM_004738.5(VAPB):c.*1282A>G rs1802459 0.15337
NM_004738.5(VAPB):c.*937G>C rs1059794 0.11399
NM_004738.5(VAPB):c.*4520T>C rs763514 0.10837
NM_004738.5(VAPB):c.*1265G>C rs7400 0.09272
NM_004738.5(VAPB):c.*2819A>G rs74568509 0.08036
NM_004738.5(VAPB):c.*4446G>A rs79623348 0.06497
NM_004738.5(VAPB):c.*4868C>T rs74748993 0.05916
NM_004738.5(VAPB):c.*4052C>T rs76295834 0.05914
NM_004738.5(VAPB):c.*4952C>T rs116665485 0.01608
NM_004738.5(VAPB):c.*6182C>T rs76708676 0.01132
NM_004738.5(VAPB):c.*6088C>T rs147304840 0.00734
NM_004738.5(VAPB):c.*753C>G rs6070466 0.00707
NM_004738.5(VAPB):c.*1641G>A rs116584680 0.00529
NM_004738.5(VAPB):c.*6619G>A rs79091887 0.00520
NM_004738.5(VAPB):c.*995T>G rs76895132 0.00501
NM_004738.5(VAPB):c.*4559A>G rs73296848 0.00228
NM_004738.5(VAPB):c.*1773G>A rs75999456 0.00188
NM_004738.5(VAPB):c.*2671A>G rs115191022 0.00183
NM_004738.5(VAPB):c.*3968C>T rs149967447 0.00183
NM_004738.5(VAPB):c.510G>A (p.Met170Ile) rs143144050 0.00170
NM_004738.5(VAPB):c.*2320T>A rs181028077 0.00163
NM_004738.5(VAPB):c.*4072C>T rs190652187 0.00163
NM_004738.5(VAPB):c.*1413C>G rs190582293 0.00139
NM_004738.5(VAPB):c.316-17A>C rs201335617 0.00115
NM_004738.5(VAPB):c.*75G>A rs138521885 0.00098
NM_004738.5(VAPB):c.*3822C>G rs150825395 0.00093
NM_004738.5(VAPB):c.*2224C>T rs189009703 0.00073
NM_004738.5(VAPB):c.*2766C>T rs6128346 0.00064
NM_004738.5(VAPB):c.390T>G (p.Asp130Glu) rs146459055 0.00059
NM_004738.5(VAPB):c.*3020A>G rs570716807 0.00053
NM_004738.5(VAPB):c.59-4A>G rs193136039 0.00044
NM_004738.5(VAPB):c.*596C>T rs118055109 0.00036
NM_004738.5(VAPB):c.*5005T>A rs146687585 0.00027
NM_004738.5(VAPB):c.*2592G>A rs143902869 0.00023
NM_004738.5(VAPB):c.105G>A (p.Pro35=) rs141383583 0.00023
NM_004738.5(VAPB):c.528G>A (p.Leu176=) rs199921117 0.00022
NM_004738.5(VAPB):c.*1335C>T rs187441988 0.00014
NM_004738.5(VAPB):c.*4923A>G rs776329339 0.00006
NM_004738.5(VAPB):c.574-5C>T rs200211497 0.00006
NM_004738.5(VAPB):c.*884A>G rs3746398 0.00004
NM_004738.5(VAPB):c.*4240G>C rs554043472 0.00001
NM_004738.5(VAPB):c.681G>A (p.Leu227=) rs778389082 0.00001
NM_004738.5(VAPB):c.*5612C>G rs140602757
NM_004738.5(VAPB):c.-33C>G rs201547974
NM_004738.5(VAPB):c.156C>T (p.Tyr52=) rs749580878
NM_004738.5(VAPB):c.316-3del
NM_004738.5(VAPB):c.59-20G>A

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.