ClinVar Miner

List of variants in gene GCK reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 16
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NM_000162.5(GCK):c.*11C>T rs200698755
NM_000162.5(GCK):c.1019+18G>A rs150914617
NM_000162.5(GCK):c.1253+8C>T rs2908274
NM_000162.5(GCK):c.129C>T (p.Arg43=) rs760912915
NM_000162.5(GCK):c.1317C>T (p.Ile439=) rs1554334455
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.31G>A (p.Ala11Thr) rs116093166
NM_000162.5(GCK):c.333C>T (p.Pro111=) rs61736250
NM_000162.5(GCK):c.364-18A>G rs191255582
NM_000162.5(GCK):c.46-12C>T rs142829768
NM_000162.5(GCK):c.483+14A>G rs74852379
NM_000162.5(GCK):c.618G>A (p.Thr206=) rs142817246
NM_000162.5(GCK):c.660C>T (p.Cys220=) rs142952813
NM_000162.5(GCK):c.9C>T (p.Asp3=) rs142553382

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