ClinVar Miner

List of variants in gene SLC35C1 reported as likely benign for Leukocyte adhesion deficiency type II

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 116
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_018389.5(SLC35C1):c.*1208G>A rs115509471 0.00851
NM_018389.5(SLC35C1):c.1054C>T (p.Pro352Ser) rs145613857 0.00381
NM_018389.4(SLC35C1):c.-665C>T rs530622849 0.00288
NM_018389.5(SLC35C1):c.598G>A (p.Val200Ile) rs146971634 0.00109
NM_018389.5(SLC35C1):c.*1569G>C rs139986610 0.00108
NM_018389.5(SLC35C1):c.748G>A (p.Gly250Arg) rs148606857 0.00073
NM_018389.5(SLC35C1):c.747C>T (p.Leu249=) rs567642788 0.00013
NM_018389.5(SLC35C1):c.663G>A (p.Pro221=) rs111773874 0.00012
NM_018389.5(SLC35C1):c.975G>A (p.Thr325=) rs377098836 0.00010
NM_018389.5(SLC35C1):c.879G>A (p.Pro293=) rs573349525 0.00009
NM_018389.5(SLC35C1):c.585G>A (p.Ser195=) rs750284604 0.00007
NM_018389.5(SLC35C1):c.597C>T (p.Thr199=) rs376082724 0.00007
NM_018389.5(SLC35C1):c.130G>A (p.Val44Met) rs541937245 0.00006
NM_018389.5(SLC35C1):c.903G>T (p.Thr301=) rs150743224 0.00006
NM_018389.5(SLC35C1):c.606C>T (p.Gly202=) rs757590578 0.00005
NM_018389.5(SLC35C1):c.29G>A (p.Arg10Lys) rs567155861 0.00004
NM_018389.5(SLC35C1):c.705C>T (p.Asn235=) rs747383355 0.00004
NM_018389.5(SLC35C1):c.153C>G (p.Thr51=) rs773263009 0.00003
NM_018389.5(SLC35C1):c.255G>A (p.Thr85=) rs374975158 0.00003
NM_018389.5(SLC35C1):c.291C>T (p.Cys97=) rs1263733426 0.00003
NM_018389.5(SLC35C1):c.309C>T (p.Asp103=) rs189405956 0.00003
NM_018389.5(SLC35C1):c.567G>C (p.Gly189=) rs763541662 0.00003
NM_018389.5(SLC35C1):c.633C>G (p.Leu211=) rs372353822 0.00003
NM_018389.5(SLC35C1):c.645C>T (p.Tyr215=) rs200626011 0.00003
NM_018389.5(SLC35C1):c.711C>T (p.Asn237=) rs777163801 0.00003
NM_018389.5(SLC35C1):c.742C>T (p.Leu248=) rs774081262 0.00003
NM_018389.5(SLC35C1):c.858G>A (p.Leu286=) rs769671439 0.00003
NM_018389.5(SLC35C1):c.1080C>T (p.Ser360=) rs749987181 0.00002
NM_018389.5(SLC35C1):c.330C>T (p.Asp110=) rs374967002 0.00002
NM_018389.5(SLC35C1):c.51C>T (p.Thr17=) rs768517924 0.00002
NM_018389.5(SLC35C1):c.636C>T (p.Asn212=) rs549069990 0.00002
NM_018389.5(SLC35C1):c.897G>A (p.Ser299=) rs141170131 0.00002
NM_018389.5(SLC35C1):c.939C>T (p.Leu313=) rs776684184 0.00002
NM_018389.5(SLC35C1):c.1005C>T (p.Ser335=) rs758133617 0.00001
NM_018389.5(SLC35C1):c.108G>A (p.Leu36=) rs779390849 0.00001
NM_018389.5(SLC35C1):c.126G>C (p.Ala42=) rs746706225 0.00001
NM_018389.5(SLC35C1):c.231C>G (p.Thr77=) rs1162234989 0.00001
NM_018389.5(SLC35C1):c.312C>T (p.Phe104=) rs75224835 0.00001
NM_018389.5(SLC35C1):c.336G>A (p.Arg112=) rs1348372856 0.00001
NM_018389.5(SLC35C1):c.345C>T (p.Arg115=) rs1207351026 0.00001
NM_018389.5(SLC35C1):c.354G>A (p.Leu118=) rs777637034 0.00001
NM_018389.5(SLC35C1):c.372C>T (p.Phe124=) rs1172535420 0.00001
NM_018389.5(SLC35C1):c.447C>T (p.Leu149=) rs2085874654 0.00001
NM_018389.5(SLC35C1):c.453C>T (p.Thr151=) rs1166821086 0.00001
NM_018389.5(SLC35C1):c.495C>T (p.Thr165=) rs1218424425 0.00001
NM_018389.5(SLC35C1):c.501C>T (p.Ser167=) rs956237776 0.00001
NM_018389.5(SLC35C1):c.535+20A>G rs2085877757 0.00001
NM_018389.5(SLC35C1):c.536-10C>G rs759978339 0.00001
NM_018389.5(SLC35C1):c.580C>T (p.Leu194=) rs764852514 0.00001
NM_018389.5(SLC35C1):c.60A>G (p.Ser20=) rs1185864574 0.00001
NM_018389.5(SLC35C1):c.630G>A (p.Ser210=) rs200577486 0.00001
NM_018389.5(SLC35C1):c.666G>A (p.Ala222=) rs754930082 0.00001
NM_018389.5(SLC35C1):c.78A>G (p.Ala26=) rs112575013 0.00001
NM_018389.5(SLC35C1):c.819C>T (p.Gly273=) rs774033676 0.00001
NM_018389.5(SLC35C1):c.837C>T (p.Ala279=) rs371692301 0.00001
NM_018389.5(SLC35C1):c.846C>T (p.Tyr282=) rs748113243 0.00001
NM_018389.5(SLC35C1):c.924A>G (p.Thr308=) rs1489703407 0.00001
NM_018389.5(SLC35C1):c.933C>T (p.Ala311=) rs1025394775 0.00001
NM_018389.5(SLC35C1):c.945C>T (p.Tyr315=) rs774226494 0.00001
NM_018389.5(SLC35C1):c.954C>G (p.Thr318=) rs767630837 0.00001
NM_018389.5(SLC35C1):c.*1636G>T rs79173599
NM_018389.5(SLC35C1):c.1002C>A (p.Ser334=)
NM_018389.5(SLC35C1):c.1008C>T (p.Ala336=) rs2134598644
NM_018389.5(SLC35C1):c.123C>T (p.Ile41=) rs1590742957
NM_018389.5(SLC35C1):c.12C>T (p.Ala4=) rs2085864611
NM_018389.5(SLC35C1):c.150C>T (p.Val50=) rs1437969304
NM_018389.5(SLC35C1):c.183C>T (p.Tyr61=) rs2085868285
NM_018389.5(SLC35C1):c.198C>T (p.Pro66=) rs1358909221
NM_018389.5(SLC35C1):c.204G>A (p.Leu68=) rs2085868809
NM_018389.5(SLC35C1):c.207G>A (p.Arg69=) rs757588395
NM_018389.5(SLC35C1):c.213C>T (p.Asp71=)
NM_018389.5(SLC35C1):c.216C>T (p.Thr72=) rs750960775
NM_018389.5(SLC35C1):c.222C>A (p.Ile74=) rs2494692554
NM_018389.5(SLC35C1):c.255G>T (p.Thr85=) rs374975158
NM_018389.5(SLC35C1):c.258G>A (p.Leu86=) rs2494692742
NM_018389.5(SLC35C1):c.285C>A (p.Ala95=)
NM_018389.5(SLC35C1):c.303C>T (p.Ala101=) rs1252172682
NM_018389.5(SLC35C1):c.348C>T (p.Ser116=) rs755762331
NM_018389.5(SLC35C1):c.357C>T (p.Pro119=) rs2494693337
NM_018389.5(SLC35C1):c.358C>T (p.Leu120=)
NM_018389.5(SLC35C1):c.360G>A (p.Leu120=) rs1200636117
NM_018389.5(SLC35C1):c.363G>A (p.Ser121=) rs749027464
NM_018389.5(SLC35C1):c.366G>T (p.Val122=)
NM_018389.5(SLC35C1):c.402C>T (p.Cys134=) rs955606062
NM_018389.5(SLC35C1):c.408G>A (p.Lys136=) rs1297705723
NM_018389.5(SLC35C1):c.411C>T (p.Tyr137=) rs1307540035
NM_018389.5(SLC35C1):c.516C>T (p.Leu172=)
NM_018389.5(SLC35C1):c.519C>G (p.Thr173=)
NM_018389.5(SLC35C1):c.535+11del
NM_018389.5(SLC35C1):c.535+15G>A
NM_018389.5(SLC35C1):c.536-16C>T rs1285699012
NM_018389.5(SLC35C1):c.536-21CTC[2] rs771937822
NM_018389.5(SLC35C1):c.540C>T (p.Gly180=)
NM_018389.5(SLC35C1):c.549T>C (p.Leu183=) rs2494704944
NM_018389.5(SLC35C1):c.564G>A (p.Glu188=) rs543075977
NM_018389.5(SLC35C1):c.573A>G (p.Glu191=)
NM_018389.5(SLC35C1):c.603C>T (p.Phe201=) rs1273640632
NM_018389.5(SLC35C1):c.651G>A (p.Thr217=)
NM_018389.5(SLC35C1):c.651G>T (p.Thr217=) rs138126275
NM_018389.5(SLC35C1):c.66C>T (p.Pro22=) rs1326280684
NM_018389.5(SLC35C1):c.672C>T (p.Asp224=) rs528291665
NM_018389.5(SLC35C1):c.717_718inv (p.Ile240Val)
NM_018389.5(SLC35C1):c.738C>G (p.Leu246=) rs369955835
NM_018389.5(SLC35C1):c.738C>T (p.Leu246=) rs369955835
NM_018389.5(SLC35C1):c.744G>T (p.Leu248=) rs1352651416
NM_018389.5(SLC35C1):c.759G>A (p.Gln253=) rs750469107
NM_018389.5(SLC35C1):c.804G>T (p.Gly268=) rs1327025697
NM_018389.5(SLC35C1):c.840C>A (p.Ile280=) rs368103927
NM_018389.5(SLC35C1):c.840C>T (p.Ile280=) rs368103927
NM_018389.5(SLC35C1):c.84C>A (p.Ala28=) rs1427324247
NM_018389.5(SLC35C1):c.861G>A (p.Gln287=) rs2494706898
NM_018389.5(SLC35C1):c.885C>T (p.Thr295=) rs2085940105
NM_018389.5(SLC35C1):c.903G>A (p.Thr301=) rs150743224
NM_018389.5(SLC35C1):c.933C>G (p.Ala311=) rs1025394775
NM_018389.5(SLC35C1):c.978C>T (p.Ser326=) rs2494707439
NM_018389.5(SLC35C1):c.996C>T (p.Gly332=)

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.