ClinVar Miner

List of variants in gene GCK reported as uncertain significance

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 108
Download table as spreadsheet
HGVS dbSNP
GCK:c.864-159_864-149del rs386134235
NM_000162.3(GCK):c.364-35dupC rs193922293
NM_000162.3(GCK):c.364-48dupC rs193922294
NM_000162.3(GCK):c.680-91dupG rs193922321
NM_000162.4(GCK):c.-470-17C>G rs1329261791
NM_000162.5(GCK):c.*270C>T rs886062348
NM_000162.5(GCK):c.*548G>A rs886062347
NM_000162.5(GCK):c.*721C>T rs886062346
NM_000162.5(GCK):c.*723A>G rs886062345
NM_000162.5(GCK):c.*844A>C rs886062344
NM_000162.5(GCK):c.-102G>A rs781377703
NM_000162.5(GCK):c.-135G>A rs746492953
NM_000162.5(GCK):c.-17C>T rs190731555
NM_000162.5(GCK):c.-452G>A rs187173652
NM_000162.5(GCK):c.-453C>T rs191795044
NM_000162.5(GCK):c.-5T>C rs193922251
NM_000162.5(GCK):c.1019+16G>A rs193922256
NM_000162.5(GCK):c.1020-10C>A rs193922257
NM_000162.5(GCK):c.1030G>T (p.Asp344Tyr) rs1131692257
NM_000162.5(GCK):c.1113C>G (p.Cys371Trp) rs556581174
NM_000162.5(GCK):c.1120G>A (p.Val374Met) rs1415041911
NM_000162.5(GCK):c.1129C>T (p.Arg377Cys) rs1471992838
NM_000162.5(GCK):c.1130G>A (p.Arg377His) rs193922264
NM_000162.5(GCK):c.1130_1138del (p.Arg377_Ala379del) rs1131691505
NM_000162.5(GCK):c.1136C>A (p.Ala379Glu) rs193922265
NM_000162.5(GCK):c.1136C>G (p.Ala379Gly) rs193922265
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.1144T>C (p.Cys382Arg) rs1554334613
NM_000162.5(GCK):c.1174C>T (p.Arg392Cys) rs1167124132
NM_000162.5(GCK):c.1229G>A (p.Gly410Asp) rs1554334546
NM_000162.5(GCK):c.1235T>G (p.Val412Gly) rs1554334539
NM_000162.5(GCK):c.124G>C (p.Asp42His) rs1562719786
NM_000162.5(GCK):c.1255T>C (p.Phe419Leu) rs1554334478
NM_000162.5(GCK):c.1268T>C (p.Phe423Ser) rs193922273
NM_000162.5(GCK):c.1280T>G (p.Val427Gly) rs1562712097
NM_000162.5(GCK):c.1288C>T (p.Leu430=) rs193922276
NM_000162.5(GCK):c.1310C>T (p.Thr437Ile) rs1185622190
NM_000162.5(GCK):c.1322C>T (p.Ser441Leu) rs1286804191
NM_000162.5(GCK):c.134T>C (p.Leu45Pro) rs1131691598
NM_000162.5(GCK):c.1364T>A (p.Val455Glu)
NM_000162.5(GCK):c.137G>T (p.Arg46Met) rs1064796993
NM_000162.5(GCK):c.1386G>T (p.Met462Ile) rs193922285
NM_000162.5(GCK):c.146C>A (p.Thr49Asn) rs193922286
NM_000162.5(GCK):c.187C>T (p.Arg63Cys) rs754479025
NM_000162.5(GCK):c.198A>G (p.Pro66=) rs377410513
NM_000162.5(GCK):c.208+11G>A rs77440690
NM_000162.5(GCK):c.208+16C>T rs377747439
NM_000162.5(GCK):c.208+9T>A rs193922288
NM_000162.5(GCK):c.255G>T (p.Arg85Ser) rs1554335758
NM_000162.5(GCK):c.322T>C (p.Tyr108His)
NM_000162.5(GCK):c.330C>G (p.Ile110Met) rs1554335741
NM_000162.5(GCK):c.355G>A (p.Ala119Thr) rs1064796698
NM_000162.5(GCK):c.363+10G>C rs758495950
NM_000162.5(GCK):c.363+6C>A rs751756042
NM_000162.5(GCK):c.364C>A (p.Leu122Ile) rs1554335616
NM_000162.5(GCK):c.364C>G (p.Leu122Val) rs1554335616
NM_000162.5(GCK):c.370G>A (p.Asp124Asn) rs759072800
NM_000162.5(GCK):c.370G>C (p.Asp124His) rs759072800
NM_000162.5(GCK):c.377T>C (p.Ile126Thr) rs1562718220
NM_000162.5(GCK):c.427_428delinsCT (p.Lys143Leu) rs1554335598
NM_000162.5(GCK):c.431T>C (p.Leu144Pro) rs1554335596
NM_000162.5(GCK):c.442T>A (p.Phe148Ile) rs1554335582
NM_000162.5(GCK):c.449T>A (p.Phe150Tyr) rs193922297
NM_000162.5(GCK):c.45+11C>G rs193922298
NM_000162.5(GCK):c.45+3A>G rs1554340088
NM_000162.5(GCK):c.457C>T (p.Pro153Ser) rs193922300
NM_000162.5(GCK):c.46-12C>T rs142829768
NM_000162.5(GCK):c.464G>C (p.Arg155Thr) rs1554335573
NM_000162.5(GCK):c.466C>T (p.His156Tyr) rs1562718043
NM_000162.5(GCK):c.477C>G (p.Ile159Met) rs1554335567
NM_000162.5(GCK):c.483+10G>A rs1554335560
NM_000162.5(GCK):c.499T>C (p.Trp167Arg) rs1481197092
NM_000162.5(GCK):c.523G>A (p.Gly175Arg) rs587780344
NM_000162.5(GCK):c.527C>A (p.Ala176Glu) rs193922304
NM_000162.5(GCK):c.540T>G (p.Asn180Lys) rs1554335444
NM_000162.5(GCK):c.566T>C (p.Ile189Thr) rs1554335441
NM_000162.5(GCK):c.572G>A (p.Arg191Gln) rs886042610
NM_000162.5(GCK):c.579+8G>A rs1562717232
NM_000162.5(GCK):c.580-13T>A rs1386067636
NM_000162.5(GCK):c.590T>C (p.Met197Thr) rs1554335418
NM_000162.5(GCK):c.595G>A (p.Val199Met) rs1554335417
NM_000162.5(GCK):c.601G>T (p.Ala201Ser) rs794727775
NM_000162.5(GCK):c.605T>C (p.Met202Thr) rs193922311
NM_000162.5(GCK):c.623C>T (p.Ala208Val) rs746913146
NM_000162.5(GCK):c.632T>A (p.Ile211Asn) rs1554335400
NM_000162.5(GCK):c.646G>A (p.Glu216Lys) rs778550411
NM_000162.5(GCK):c.688T>C (p.Cys230Arg) rs794727839
NM_000162.5(GCK):c.701A>G (p.Tyr234Cys) rs1562715620
NM_000162.5(GCK):c.735G>A (p.Glu245=) rs775481896
NM_000162.5(GCK):c.748C>T (p.Arg250Cys) rs1057524904
NM_000162.5(GCK):c.749G>A (p.Arg250His) rs370375148
NM_000162.5(GCK):c.74T>A (p.Leu25Gln) rs193922325
NM_000162.5(GCK):c.776C>T (p.Ala259Val) rs1554335132
NM_000162.5(GCK):c.784G>A (p.Asp262Asn) rs779460424
NM_000162.5(GCK):c.802G>A (p.Glu268Lys) rs1554335111
NM_000162.5(GCK):c.820G>C (p.Asp274His) rs1554335109
NM_000162.5(GCK):c.823C>T (p.Arg275Cys)
NM_000162.5(GCK):c.824G>A (p.Arg275His) rs767565869
NM_000162.5(GCK):c.830T>G (p.Val277Gly) rs1554335093
NM_000162.5(GCK):c.835G>C (p.Glu279Gln) rs104894005
NM_000162.5(GCK):c.863+3A>G rs193922334
NM_000162.5(GCK):c.883G>A (p.Gly295Ser) rs1554334905
NM_000162.5(GCK):c.918_919delinsAT (p.Leu307Phe) rs1057524892
NM_000162.5(GCK):c.951C>G (p.His317Gln) rs1379908545
NM_000162.5(GCK):c.989T>C (p.Phe330Ser) rs1554334872
NM_000162.5(GCK):c.995C>G (p.Thr332Arg) rs770231054
NM_033507.2(GCK):c.1030G>T (p.Gly344Cys) rs1131692257

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.