ClinVar Miner

List of variants in gene GCK reported as uncertain significance for not specified

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Gene type:
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Total variants: 79
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HGVS dbSNP gnomAD frequency
NM_000162.5(GCK):c.-455A>G rs140894490 0.00101
NM_000162.5(GCK):c.-453C>T rs191795044 0.00049
NM_000162.5(GCK):c.-98C>T rs200216829 0.00024
NM_000162.5(GCK):c.-102G>A rs781377703 0.00023
NM_000162.5(GCK):c.208+16C>T rs377747439 0.00018
NM_000162.5(GCK):c.-17C>T rs190731555 0.00017
NM_000162.5(GCK):c.735G>A (p.Glu245=) rs775481896 0.00016
NM_000162.5(GCK):c.1288C>T (p.Leu430=) rs193922276 0.00013
NM_000162.5(GCK):c.-299A>G rs765620490 0.00012
NM_000162.5(GCK):c.-375C>T rs775776110 0.00009
NM_000162.5(GCK):c.363+6C>A rs751756042 0.00004
NM_000162.5(GCK):c.-135G>A rs746492953 0.00003
NM_000162.5(GCK):c.142G>A (p.Glu48Lys) rs759514960 0.00003
NM_000162.3(GCK):c.-487C>G rs1329261791 0.00002
NM_000162.5(GCK):c.-452G>A rs187173652 0.00002
NM_000162.5(GCK):c.394G>A (p.Asp132Asn) rs762419802 0.00002
NM_000162.5(GCK):c.784G>A (p.Asp262Asn) rs779460424 0.00002
NM_000162.3(GCK):c.-534C>T rs182891400 0.00001
NM_000162.5(GCK):c.1386G>T (p.Met462Ile) rs193922285 0.00001
NM_000162.5(GCK):c.187C>T (p.Arg63Cys) rs754479025 0.00001
NM_000162.5(GCK):c.499T>C (p.Trp167Arg) rs1481197092 0.00001
NM_000162.5(GCK):c.605T>C (p.Met202Thr) rs193922311 0.00001
NM_000162.5(GCK):c.824G>A (p.Arg275His) rs767565869 0.00001
NM_000162.5(GCK):c.951C>G (p.His317Gln) rs1379908545 0.00001
NM_000162.5(GCK):c.1012G>A (p.Val338Met)
NM_000162.5(GCK):c.1020-10C>A rs193922257
NM_000162.5(GCK):c.1033C>G (p.Arg345Gly) rs2096271919
NM_000162.5(GCK):c.1064T>C (p.Leu355Pro) rs1583592156
NM_000162.5(GCK):c.1120G>A (p.Val374Met) rs1415041911
NM_000162.5(GCK):c.1130G>A (p.Arg377His) rs193922264
NM_000162.5(GCK):c.1130G>T (p.Arg377Leu) rs193922264
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.1207C>G (p.Arg403Gly) rs193922271
NM_000162.5(GCK):c.1222G>A (p.Val408Met) rs1293307672
NM_000162.5(GCK):c.1235T>G (p.Val412Gly) rs1554334539
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.1298_1309del (p.Ser433_Ile436del)
NM_000162.5(GCK):c.1309A>C (p.Thr437Pro) rs2096270595
NM_000162.5(GCK):c.130G>T (p.Gly44Cys)
NM_000162.5(GCK):c.1319A>G (p.Glu440Gly) rs2128818815
NM_000162.5(GCK):c.1331G>A (p.Gly444Asp)
NM_000162.5(GCK):c.167A>C (p.Lys56Thr)
NM_000162.5(GCK):c.179C>T (p.Thr60Ile) rs747783371
NM_000162.5(GCK):c.207A>G (p.Ser69=) rs779548342
NM_000162.5(GCK):c.323A>G (p.Tyr108Cys)
NM_000162.5(GCK):c.330C>G (p.Ile110Met) rs1554335741
NM_000162.5(GCK):c.350G>T (p.Gly117Val)
NM_000162.5(GCK):c.397T>C (p.Phe133Leu) rs2128822093
NM_000162.5(GCK):c.422A>C (p.His141Pro) rs2128822078
NM_000162.5(GCK):c.423C>A (p.His141Gln) rs1299283674
NM_000162.5(GCK):c.440G>A (p.Gly147Asp) rs193922296
NM_000162.5(GCK):c.442T>A (p.Phe148Ile) rs1554335582
NM_000162.5(GCK):c.457C>T (p.Pro153Ser) rs193922300
NM_000162.5(GCK):c.45G>A (p.Lys15=)
NM_000162.5(GCK):c.464G>C (p.Arg155Thr) rs1554335573
NM_000162.5(GCK):c.477C>G (p.Ile159Met) rs1554335567
NM_000162.5(GCK):c.483+10G>A rs1554335560
NM_000162.5(GCK):c.551T>C (p.Leu184Pro) rs2128821610
NM_000162.5(GCK):c.565A>G (p.Ile189Val)
NM_000162.5(GCK):c.567C>G (p.Ile189Met)
NM_000162.5(GCK):c.590T>C (p.Met197Thr) rs1554335418
NM_000162.5(GCK):c.632T>A (p.Ile211Asn) rs1554335400
NM_000162.5(GCK):c.680-15C>A rs369345791
NM_000162.5(GCK):c.688T>C (p.Cys230Arg) rs794727839
NM_000162.5(GCK):c.691A>G (p.Asn231Asp) rs2128820674
NM_000162.5(GCK):c.737G>A (p.Gly246Glu) rs1583596522
NM_000162.5(GCK):c.749G>A (p.Arg250His) rs370375148
NM_000162.5(GCK):c.776C>T (p.Ala259Val) rs1554335132
NM_000162.5(GCK):c.808CTG[1] (p.Leu271del) rs2096275478
NM_000162.5(GCK):c.820G>C (p.Asp274His) rs1554335109
NM_000162.5(GCK):c.823C>G (p.Arg275Gly)
NM_000162.5(GCK):c.830T>G (p.Val277Gly) rs1554335093
NM_000162.5(GCK):c.835G>A (p.Glu279Lys) rs104894005
NM_000162.5(GCK):c.835G>C (p.Glu279Gln) rs104894005
NM_000162.5(GCK):c.864G>C (p.Leu288=) rs2128820056
NM_000162.5(GCK):c.883G>A (p.Gly295Ser) rs1554334905
NM_000162.5(GCK):c.981C>G (p.Arg327=) rs766907428

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