ClinVar Miner

List of variants in gene GCK reported as uncertain significance by Invitae

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Gene type:
ClinVar version:
Total variants: 165
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HGVS dbSNP gnomAD frequency
NM_000162.5(GCK):c.-457C>T rs548039601 0.00011
NM_000162.5(GCK):c.649G>A (p.Asp217Asn) rs147065275 0.00011
NM_000162.5(GCK):c.646G>A (p.Glu216Lys) rs778550411 0.00004
NM_000162.5(GCK):c.836A>G (p.Glu279Gly) rs143484733 0.00004
NM_000162.5(GCK):c.301G>A (p.Val101Met) rs762922697 0.00003
NM_000162.5(GCK):c.10G>A (p.Asp4Asn) rs202091228 0.00002
NM_000162.5(GCK):c.483+3G>A rs1311596702 0.00002
NM_000162.5(GCK):c.784G>A (p.Asp262Asn) rs779460424 0.00002
NM_000162.5(GCK):c.1042A>T (p.Ile348Phe) rs193922260 0.00001
NM_000162.5(GCK):c.107G>A (p.Arg36Gln) rs193922261 0.00001
NM_000162.5(GCK):c.1324G>A (p.Glu442Lys) rs758737171 0.00001
NM_000162.5(GCK):c.1364T>A (p.Val455Glu) rs753795627 0.00001
NM_000162.5(GCK):c.755G>T (p.Cys252Phe) rs1372204515 0.00001
NM_000162.5(GCK):c.757G>A (p.Val253Ile) rs748964205 0.00001
NM_000162.5(GCK):c.908G>A (p.Arg303Gln) rs1312678560 0.00001
NM_000162.5(GCK):c.1004T>A (p.Val335Glu)
NM_000162.5(GCK):c.1013T>G (p.Val338Gly)
NM_000162.5(GCK):c.1014G>A (p.Val338=)
NM_000162.5(GCK):c.1018A>G (p.Ser340Gly) rs193922255
NM_000162.5(GCK):c.1019G>A (p.Ser340Asn) rs1376631949
NM_000162.5(GCK):c.1020-16T>A
NM_000162.5(GCK):c.1033C>G (p.Arg345Gly) rs2096271919
NM_000162.5(GCK):c.1079C>G (p.Ser360Trp)
NM_000162.5(GCK):c.1093G>A (p.Asp365Asn)
NM_000162.5(GCK):c.1108G>C (p.Ala370Pro)
NM_000162.5(GCK):c.1111T>G (p.Cys371Gly)
NM_000162.5(GCK):c.1112G>T (p.Cys371Phe) rs587780343
NM_000162.5(GCK):c.1113C>G (p.Cys371Trp) rs556581174
NM_000162.5(GCK):c.1124C>A (p.Ser375Tyr)
NM_000162.5(GCK):c.1129C>A (p.Arg377Ser)
NM_000162.5(GCK):c.1132G>A (p.Ala378Thr) rs104894016
NM_000162.5(GCK):c.1133C>G (p.Ala378Gly) rs193929374
NM_000162.5(GCK):c.1133C>T (p.Ala378Val) rs193929374
NM_000162.5(GCK):c.113A>C (p.Gln38Pro) rs1064794268
NM_000162.5(GCK):c.1142T>A (p.Met381Lys) rs193922266
NM_000162.5(GCK):c.1151C>A (p.Ala384Glu)
NM_000162.5(GCK):c.1151C>T (p.Ala384Val) rs1583591747
NM_000162.5(GCK):c.1153G>C (p.Gly385Arg)
NM_000162.5(GCK):c.1156C>G (p.Leu386Val) rs1583591700
NM_000162.5(GCK):c.1157T>C (p.Leu386Pro) rs193922268
NM_000162.5(GCK):c.115_117del (p.Lys39del) rs2096283216
NM_000162.5(GCK):c.1160C>T (p.Ala387Val) rs193921338
NM_000162.5(GCK):c.1163G>A (p.Gly388Asp) rs2096271482
NM_000162.5(GCK):c.1169T>A (p.Ile390Asn) rs193921340
NM_000162.5(GCK):c.1180C>T (p.Arg394Cys)
NM_000162.5(GCK):c.1181G>C (p.Arg394Pro)
NM_000162.5(GCK):c.1181G>T (p.Arg394Leu) rs1235227560
NM_000162.5(GCK):c.1184A>G (p.Glu395Gly)
NM_000162.5(GCK):c.1189C>T (p.Arg397Cys)
NM_000162.5(GCK):c.1201G>A (p.Val401Ile)
NM_000162.5(GCK):c.1217T>C (p.Val406Ala)
NM_000162.5(GCK):c.1219G>A (p.Gly407Ser) rs2096271295
NM_000162.5(GCK):c.1219G>C (p.Gly407Arg)
NM_000162.5(GCK):c.1222G>A (p.Val408Met) rs1293307672
NM_000162.5(GCK):c.1228G>C (p.Gly410Arg) rs2128819136
NM_000162.5(GCK):c.1235T>C (p.Val412Ala)
NM_000162.5(GCK):c.1254-1G>A
NM_000162.5(GCK):c.1264C>G (p.Arg422Gly)
NM_000162.5(GCK):c.1271A>C (p.His424Pro) rs2128818866
NM_000162.5(GCK):c.1297_1311del (p.Ser433_Thr437del)
NM_000162.5(GCK):c.130G>T (p.Gly44Cys)
NM_000162.5(GCK):c.1310C>T (p.Thr437Ile) rs1185622190
NM_000162.5(GCK):c.1327G>A (p.Glu443Lys)
NM_000162.5(GCK):c.1331G>A (p.Gly444Asp)
NM_000162.5(GCK):c.1335T>A (p.Ser445Arg) rs2128818794
NM_000162.5(GCK):c.1340_1368del (p.Arg447fs) rs1339598338
NM_000162.5(GCK):c.1348G>T (p.Ala450Ser)
NM_000162.5(GCK):c.1349C>T (p.Ala450Val)
NM_000162.5(GCK):c.134T>C (p.Leu45Pro) rs1131691598
NM_000162.5(GCK):c.1358C>G (p.Ser453Trp)
NM_000162.5(GCK):c.146C>G (p.Thr49Ser)
NM_000162.5(GCK):c.146C>T (p.Thr49Ile) rs193922286
NM_000162.5(GCK):c.167A>C (p.Lys56Thr)
NM_000162.5(GCK):c.181T>A (p.Tyr61Asn) rs2128823113
NM_000162.5(GCK):c.188G>A (p.Arg63His)
NM_000162.5(GCK):c.188G>T (p.Arg63Leu) rs746444094
NM_000162.5(GCK):c.208+9T>A rs193922288
NM_000162.5(GCK):c.215G>A (p.Gly72Glu) rs2128822720
NM_000162.5(GCK):c.251T>C (p.Phe84Ser) rs2128822702
NM_000162.5(GCK):c.301G>T (p.Val101Leu)
NM_000162.5(GCK):c.314A>G (p.His105Arg)
NM_000162.5(GCK):c.329T>G (p.Ile110Ser) rs1338970607
NM_000162.5(GCK):c.332C>T (p.Pro111Leu)
NM_000162.5(GCK):c.334G>A (p.Glu112Lys)
NM_000162.5(GCK):c.349G>C (p.Gly117Arg) rs748554061
NM_000162.5(GCK):c.352A>T (p.Thr118Ser)
NM_000162.5(GCK):c.355G>A (p.Ala119Thr) rs1064796698
NM_000162.5(GCK):c.364C>A (p.Leu122Ile) rs1554335616
NM_000162.5(GCK):c.365T>C (p.Leu122Pro)
NM_000162.5(GCK):c.368T>C (p.Phe123Ser)
NM_000162.5(GCK):c.370G>C (p.Asp124His) rs759072800
NM_000162.5(GCK):c.371A>T (p.Asp124Val) rs1554335612
NM_000162.5(GCK):c.379T>G (p.Ser127Ala)
NM_000162.5(GCK):c.388A>T (p.Ile130Phe) rs2128822105
NM_000162.5(GCK):c.389T>C (p.Ile130Thr)
NM_000162.5(GCK):c.397T>A (p.Phe133Ile)
NM_000162.5(GCK):c.397T>C (p.Phe133Leu) rs2128822093
NM_000162.5(GCK):c.430C>G (p.Leu144Val)
NM_000162.5(GCK):c.440G>A (p.Gly147Asp) rs193922296
NM_000162.5(GCK):c.449T>A (p.Phe150Tyr) rs193922297
NM_000162.5(GCK):c.44A>G (p.Lys15Arg)
NM_000162.5(GCK):c.45G>A (p.Lys15=)
NM_000162.5(GCK):c.46-3C>G rs1413094138
NM_000162.5(GCK):c.46-3C>T
NM_000162.5(GCK):c.463A>G (p.Arg155Gly) rs193922301
NM_000162.5(GCK):c.465G>T (p.Arg155Ser)
NM_000162.5(GCK):c.476T>A (p.Ile159Asn)
NM_000162.5(GCK):c.476T>C (p.Ile159Thr)
NM_000162.5(GCK):c.478G>A (p.Asp160Asn) rs1554335566
NM_000162.5(GCK):c.48_50del (p.Glu17del) rs2128823241
NM_000162.5(GCK):c.491T>C (p.Leu164Pro) rs2096278847
NM_000162.5(GCK):c.503C>T (p.Thr168Ile) rs2096278825
NM_000162.5(GCK):c.526G>A (p.Ala176Thr)
NM_000162.5(GCK):c.531A>C (p.Glu177Asp)
NM_000162.5(GCK):c.539A>G (p.Asn180Ser)
NM_000162.5(GCK):c.542T>C (p.Val181Ala) rs193922306
NM_000162.5(GCK):c.551T>C (p.Leu184Pro) rs2128821610
NM_000162.5(GCK):c.568A>G (p.Lys190Glu)
NM_000162.5(GCK):c.56T>A (p.Ile19Asn)
NM_000162.5(GCK):c.598G>C (p.Val200Leu)
NM_000162.5(GCK):c.610A>G (p.Asn204Asp) rs2128821512
NM_000162.5(GCK):c.615C>G (p.Asp205Glu) rs193922312
NM_000162.5(GCK):c.627GAT[3] (p.Met210_Ile211insMet)
NM_000162.5(GCK):c.632T>A (p.Ile211Asn) rs1554335400
NM_000162.5(GCK):c.638G>A (p.Cys213Tyr)
NM_000162.5(GCK):c.638_640del (p.Cys213del) rs1583599241
NM_000162.5(GCK):c.659G>T (p.Cys220Phe)
NM_000162.5(GCK):c.666C>A (p.Val222=)
NM_000162.5(GCK):c.668G>T (p.Gly223Val)
NM_000162.5(GCK):c.671T>C (p.Met224Thr) rs2128821476
NM_000162.5(GCK):c.674T>C (p.Ile225Thr) rs2128821473
NM_000162.5(GCK):c.675C>G (p.Ile225Met) rs772754004
NM_000162.5(GCK):c.679G>A (p.Gly227Ser)
NM_000162.5(GCK):c.680-15C>A rs369345791
NM_000162.5(GCK):c.685G>A (p.Gly229Ser)
NM_000162.5(GCK):c.688T>C (p.Cys230Arg) rs794727839
NM_000162.5(GCK):c.698_700del (p.Cys233del)
NM_000162.5(GCK):c.704T>C (p.Met235Thr) rs193922323
NM_000162.5(GCK):c.717G>C (p.Gln239His) rs2128820660
NM_000162.5(GCK):c.719A>C (p.Asn240Thr)
NM_000162.5(GCK):c.731T>A (p.Val244Glu)
NM_000162.5(GCK):c.74T>G (p.Leu25Arg) rs193922325
NM_000162.5(GCK):c.756C>G (p.Cys252Trp)
NM_000162.5(GCK):c.758T>C (p.Val253Ala) rs193921400
NM_000162.5(GCK):c.762T>G (p.Asn254Lys) rs1554335141
NM_000162.5(GCK):c.772G>A (p.Gly258Ser) rs1583596378
NM_000162.5(GCK):c.776C>A (p.Ala259Asp) rs1554335132
NM_000162.5(GCK):c.802G>A (p.Glu268Lys) rs1554335111
NM_000162.5(GCK):c.809T>A (p.Leu270Gln)
NM_000162.5(GCK):c.809T>C (p.Leu270Pro) rs1583596227
NM_000162.5(GCK):c.830T>A (p.Val277Glu)
NM_000162.5(GCK):c.835G>A (p.Glu279Lys) rs104894005
NM_000162.5(GCK):c.851C>T (p.Pro284Leu)
NM_000162.5(GCK):c.864G>C (p.Leu288=) rs2128820056
NM_000162.5(GCK):c.871A>G (p.Lys291Glu) rs193922335
NM_000162.5(GCK):c.880G>C (p.Gly294Arg)
NM_000162.5(GCK):c.880G>T (p.Gly294Cys) rs2128820044
NM_000162.5(GCK):c.896G>A (p.Gly299Asp)
NM_000162.5(GCK):c.898G>A (p.Glu300Lys) rs1255911887
NM_000162.5(GCK):c.89T>C (p.Leu30Pro) rs876661320
NM_000162.5(GCK):c.917T>C (p.Leu306Pro) rs193922337
NM_000162.5(GCK):c.917T>G (p.Leu306Arg) rs193922337
NM_000162.5(GCK):c.920T>C (p.Leu307Pro)
NM_000162.5(GCK):c.946T>C (p.Phe316Leu) rs2128819989
NM_000162.5(GCK):c.98T>C (p.Val33Ala) rs1554335954

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