ClinVar Miner

List of variants reported as uncertain significance for MOGS-CDG

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 75
Download table as spreadsheet
HGVS dbSNP
NM_006302.3(MOGS):c.1024C>G (p.Gln342Glu) rs893214845
NM_006302.3(MOGS):c.103G>A (p.Gly35Ser) rs908587926
NM_006302.3(MOGS):c.1049C>G (p.Pro350Arg) rs754475101
NM_006302.3(MOGS):c.1052G>C (p.Arg351Thr) rs368536824
NM_006302.3(MOGS):c.1061G>A (p.Gly354Asp) rs200348131
NM_006302.3(MOGS):c.1072A>T (p.Thr358Ser) rs371692461
NM_006302.3(MOGS):c.1111C>T (p.Arg371Cys) rs776830090
NM_006302.3(MOGS):c.1112G>A (p.Arg371His)
NM_006302.3(MOGS):c.1124C>T (p.Thr375Ile) rs200888878
NM_006302.3(MOGS):c.1130A>G (p.Gln377Arg) rs202102671
NM_006302.3(MOGS):c.1153T>C (p.Ser385Pro)
NM_006302.3(MOGS):c.1164G>C (p.Gln388His) rs781096789
NM_006302.3(MOGS):c.116G>A (p.Ser39Asn)
NM_006302.3(MOGS):c.1201G>A (p.Gly401Arg) rs760835807
NM_006302.3(MOGS):c.1279G>T (p.Ala427Ser)
NM_006302.3(MOGS):c.1294G>A (p.Val432Ile) rs552488837
NM_006302.3(MOGS):c.1322G>A (p.Arg441Gln) rs745360345
NM_006302.3(MOGS):c.1461G>C (p.Glu487Asp) rs1240890677
NM_006302.3(MOGS):c.1484G>A (p.Arg495Gln) rs34075781
NM_006302.3(MOGS):c.1490G>A (p.Arg497Gln) rs772550239
NM_006302.3(MOGS):c.1528G>A (p.Ala510Thr) rs913447572
NM_006302.3(MOGS):c.1563T>A (p.His521Gln)
NM_006302.3(MOGS):c.1604G>A (p.Arg535Gln)
NM_006302.3(MOGS):c.169A>G (p.Met57Val)
NM_006302.3(MOGS):c.1799_1804delinsGCTCGGTCCAG (p.Leu600fs) rs1572919848
NM_006302.3(MOGS):c.1825C>T (p.Arg609Cys) rs369797433
NM_006302.3(MOGS):c.1826G>A (p.Arg609His) rs377287243
NM_006302.3(MOGS):c.1835C>T (p.Thr612Met) rs371586378
NM_006302.3(MOGS):c.183G>T (p.Trp61Cys)
NM_006302.3(MOGS):c.1851T>A (p.His617Gln) rs199939051
NM_006302.3(MOGS):c.1892C>T (p.Ala631Val) rs752324076
NM_006302.3(MOGS):c.1916G>A (p.Ser639Asn) rs1481203014
NM_006302.3(MOGS):c.1961A>T (p.Asp654Val) rs1572919705
NM_006302.3(MOGS):c.1981G>A (p.Ala661Thr)
NM_006302.3(MOGS):c.2003C>T (p.Pro668Leu)
NM_006302.3(MOGS):c.2018T>C (p.Val673Ala) rs1572919630
NM_006302.3(MOGS):c.2021G>A (p.Arg674Gln) rs200966949
NM_006302.3(MOGS):c.2033G>A (p.Arg678Gln) rs776932912
NM_006302.3(MOGS):c.2062G>A (p.Ala688Thr) rs186098891
NM_006302.3(MOGS):c.206G>A (p.Arg69Gln) rs374933674
NM_006302.3(MOGS):c.2123G>A (p.Arg708His) rs181059661
NM_006302.3(MOGS):c.2158C>T (p.Arg720Cys) rs779843206
NM_006302.3(MOGS):c.2224A>C (p.Asn742His) rs1283895621
NM_006302.3(MOGS):c.2243C>A (p.Pro748His) rs369937053
NM_006302.3(MOGS):c.2264G>T (p.Trp755Leu)
NM_006302.3(MOGS):c.2314C>A (p.Leu772Met) rs367975640
NM_006302.3(MOGS):c.2434C>T (p.Arg812Cys) rs368859958
NM_006302.3(MOGS):c.2444G>A (p.Arg815Gln) rs778832533
NM_006302.3(MOGS):c.2476A>G (p.Thr826Ala) rs1558564232
NM_006302.3(MOGS):c.2500del (p.Ala834fs) rs1296169573
NM_006302.3(MOGS):c.2505A>C (p.Glu835Asp)
NM_006302.3(MOGS):c.262C>A (p.Pro88Thr)
NM_006302.3(MOGS):c.290G>A (p.Gly97Glu) rs1572922297
NM_006302.3(MOGS):c.311A>C (p.Tyr104Ser) rs1553380245
NM_006302.3(MOGS):c.386G>A (p.Gly129Glu)
NM_006302.3(MOGS):c.397C>A (p.Leu133Ile) rs750032065
NM_006302.3(MOGS):c.436T>G (p.Tyr146Asp) rs576166441
NM_006302.3(MOGS):c.476A>T (p.Gln159Leu) rs776263791
NM_006302.3(MOGS):c.532G>A (p.Gly178Ser)
NM_006302.3(MOGS):c.562G>A (p.Val188Met) rs746611980
NM_006302.3(MOGS):c.587G>A (p.Gly196Asp) rs1257661743
NM_006302.3(MOGS):c.745A>T (p.Ser249Cys)
NM_006302.3(MOGS):c.806G>A (p.Gly269Glu) rs201775541
NM_006302.3(MOGS):c.828G>A (p.Met276Ile) rs1558566109
NM_006302.3(MOGS):c.838C>T (p.Arg280Cys)
NM_006302.3(MOGS):c.851G>A (p.Trp284Ter)
NM_006302.3(MOGS):c.858G>C (p.Gln286His) rs202095654
NM_006302.3(MOGS):c.874G>C (p.Ala292Pro)
NM_006302.3(MOGS):c.875C>A (p.Ala292Asp)
NM_006302.3(MOGS):c.886C>T (p.Arg296Cys)
NM_006302.3(MOGS):c.900G>T (p.Leu300Phe) rs886745696
NM_006302.3(MOGS):c.925A>G (p.Arg309Gly) rs1558565949
NM_006302.3(MOGS):c.947A>T (p.Gln316Leu) rs1553379896
NM_006302.3(MOGS):c.94G>A (p.Gly32Ser) rs774950414
NM_006302.3(MOGS):c.992C>T (p.Ser331Phe) rs1572920656

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.