ClinVar Miner

List of variants in gene GCK studied for carbohydrate metabolism disease

Included ClinVar conditions (161):
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Gene type:
ClinVar version:
Total variants: 70
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HGVS dbSNP
GCK, VAL91LEU
NM_000162.5(GCK):c.*11C>T rs200698755
NM_000162.5(GCK):c.*270C>T rs886062348
NM_000162.5(GCK):c.*297T>G rs527259972
NM_000162.5(GCK):c.*332G>A rs13306388
NM_000162.5(GCK):c.*356G>A rs146107173
NM_000162.5(GCK):c.*477C>T rs2908275
NM_000162.5(GCK):c.*510C>T rs141645300
NM_000162.5(GCK):c.*548G>A rs886062347
NM_000162.5(GCK):c.*678G>T rs555058443
NM_000162.5(GCK):c.*721C>T rs886062346
NM_000162.5(GCK):c.*723A>G rs886062345
NM_000162.5(GCK):c.*735C>A rs556996030
NM_000162.5(GCK):c.*764C>T rs185418856
NM_000162.5(GCK):c.*797C>T rs2908276
NM_000162.5(GCK):c.*844A>C rs886062344
NM_000162.5(GCK):c.*847G>A rs76374134
NM_000162.5(GCK):c.*92C>A rs557990162
NM_000162.5(GCK):c.-102G>A rs781377703
NM_000162.5(GCK):c.-102G>C
NM_000162.5(GCK):c.-137C>G
NM_000162.5(GCK):c.-215A>G
NM_000162.5(GCK):c.-217C>G
NM_000162.5(GCK):c.-267G>T
NM_000162.5(GCK):c.-279C>T
NM_000162.5(GCK):c.-396C>G
NM_000162.5(GCK):c.-449G>A
NM_000162.5(GCK):c.-452G>A rs187173652
NM_000162.5(GCK):c.-453C>T rs191795044
NM_000162.5(GCK):c.-455A>G
NM_000162.5(GCK):c.-456G>A
NM_000162.5(GCK):c.-84C>G
NM_000162.5(GCK):c.1024A>C (p.Thr342Pro)
NM_000162.5(GCK):c.10G>A (p.Asp4Asn)
NM_000162.5(GCK):c.1120G>T (p.Val374Leu)
NM_000162.5(GCK):c.1165G>C (p.Val389Leu) rs1350717554
NM_000162.5(GCK):c.1253+12C>T
NM_000162.5(GCK):c.1253+8C>T rs2908274
NM_000162.5(GCK):c.1262A>G (p.Glu421Gly)
NM_000162.5(GCK):c.1310C>T (p.Thr437Ile) rs1185622190
NM_000162.5(GCK):c.1358C>T (p.Ser453Leu) rs193922283
NM_000162.5(GCK):c.1358CGG[3] (p.Ala454dup) rs1554334433
NM_000162.5(GCK):c.1363G>A (p.Val455Met) rs104894012
NM_000162.5(GCK):c.1367C>T (p.Ala456Val) rs104894014
NM_000162.5(GCK):c.1386G>T (p.Met462Ile) rs193922285
NM_000162.5(GCK):c.208+11G>A rs77440690
NM_000162.5(GCK):c.209-8G>A rs144798843
NM_000162.5(GCK):c.213C>T (p.Val71=) rs143128547
NM_000162.5(GCK):c.333C>T (p.Pro111=) rs61736250
NM_000162.5(GCK):c.339C>T (p.Asp113=) rs149412035
NM_000162.5(GCK):c.363+10G>A rs758495950
NM_000162.5(GCK):c.363+10G>C rs758495950
NM_000162.5(GCK):c.363+9C>T rs200985182
NM_000162.5(GCK):c.393C>T (p.Ser131=) rs139139350
NM_000162.5(GCK):c.435C>G (p.Pro145=)
NM_000162.5(GCK):c.46-12C>T rs142829768
NM_000162.5(GCK):c.483+3G>A
NM_000162.5(GCK):c.544G>A (p.Val182Met) rs587780345
NM_000162.5(GCK):c.580-11C>T
NM_000162.5(GCK):c.618G>A (p.Thr206=) rs142817246
NM_000162.5(GCK):c.641A>G (p.Tyr214Cys) rs104894015
NM_000162.5(GCK):c.645C>T (p.Tyr215=) rs144723656
NM_000162.5(GCK):c.649G>A (p.Asp217Asn)
NM_000162.5(GCK):c.666C>T (p.Val222=) rs193922318
NM_000162.5(GCK):c.667G>A (p.Gly223Ser) rs1360415315
NM_000162.5(GCK):c.675C>T (p.Ile225=)
NM_000162.5(GCK):c.676G>A (p.Val226Met) rs148311934
NM_000162.5(GCK):c.680-14G>C
NM_000162.5(GCK):c.766G>A (p.Glu256Lys) rs769268803
NM_000162.5(GCK):c.792C>A (p.Gly264=)

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