ClinVar Miner

List of variants in gene GNE reported as likely benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
Download table as spreadsheet
HGVS dbSNP
NM_005476.7(GNE):c.-25C>T rs1158058299
NM_005476.7(GNE):c.1020A>G (p.Gln340=) rs747807631
NM_005476.7(GNE):c.102C>T (p.Thr34=) rs147290887
NM_005476.7(GNE):c.1070+7A>G rs149675783
NM_005476.7(GNE):c.1131C>T (p.Ile377=) rs764041731
NM_005476.7(GNE):c.1236T>G (p.Val412=) rs1587294795
NM_005476.7(GNE):c.1242T>C (p.Leu414=) rs371881711
NM_005476.7(GNE):c.1245C>T (p.Gly415=) rs140784655
NM_005476.7(GNE):c.1293T>A (p.Val431=) rs143485388
NM_005476.7(GNE):c.1311C>T (p.Phe437=) rs1554659051
NM_005476.7(GNE):c.1412-5C>T rs369078814
NM_005476.7(GNE):c.1509C>G (p.Pro503=) rs141172610
NM_005476.7(GNE):c.1634-4G>T rs1021602666
NM_005476.7(GNE):c.1634-7G>A rs139442869
NM_005476.7(GNE):c.165-9C>T rs760509369
NM_005476.7(GNE):c.1666T>C (p.Leu556=) rs765440649
NM_005476.7(GNE):c.1671C>T (p.Ile557=) rs1587277726
NM_005476.7(GNE):c.1716G>A (p.Val572=) rs1294027346
NM_005476.7(GNE):c.1857T>C (p.Asp619=) rs1587273465
NM_005476.7(GNE):c.1872G>A (p.Ala624=) rs145361930
NM_005476.7(GNE):c.1908G>A (p.Ala636=) rs200812140
NM_005476.7(GNE):c.2004C>T (p.Ser668=) rs150045137
NM_005476.7(GNE):c.2061C>G (p.Ala687=) rs765296741
NM_005476.7(GNE):c.2070C>T (p.Ser690=) rs776582567
NM_005476.7(GNE):c.2112C>T (p.Pro704=) rs779967033
NM_005476.7(GNE):c.2118G>A (p.Leu706=) rs1554657933
NM_005476.7(GNE):c.21C>T (p.Asn7=) rs774610596
NM_005476.7(GNE):c.297T>C (p.Leu99=) rs544304534
NM_005476.7(GNE):c.429T>C (p.Asp143=) rs1587339981
NM_005476.7(GNE):c.480C>T (p.Cys160=) rs1360990295
NM_005476.7(GNE):c.765C>T (p.Asp255=) rs775805166
NM_005476.7(GNE):c.804G>A (p.Lys268=) rs141814943
NM_005476.7(GNE):c.828T>C (p.Phe276=) rs770346895
NM_005476.7(GNE):c.831T>C (p.Arg277=) rs1367695782
NM_005476.7(GNE):c.843C>T (p.His281=) rs138694766

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.