ClinVar Miner

List of variants in gene GCK reported as likely benign

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Gene type:
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Total variants: 40
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HGVS dbSNP
NM_000162.5(GCK):c.*11C>T rs200698755
NM_000162.5(GCK):c.*297T>G rs527259972
NM_000162.5(GCK):c.*356G>A rs146107173
NM_000162.5(GCK):c.*510C>T rs141645300
NM_000162.5(GCK):c.*678G>T rs555058443
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.*847G>A rs76374134
NM_000162.5(GCK):c.*92C>A rs557990162
NM_000162.5(GCK):c.1019+18G>A rs150914617
NM_000162.5(GCK):c.117G>A (p.Lys39=) rs193922270
NM_000162.5(GCK):c.1253+8C>T rs2908274
NM_000162.5(GCK):c.1285A>C (p.Arg429=) rs140672134
NM_000162.5(GCK):c.1288C>T (p.Leu430=) rs193922276
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.208+17G>A
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.339C>T (p.Asp113=) rs149412035
NM_000162.5(GCK):c.363+10G>A rs758495950
NM_000162.5(GCK):c.364-18A>G rs191255582
NM_000162.5(GCK):c.393C>T (p.Ser131=) rs139139350
NM_000162.5(GCK):c.450C>T (p.Phe150=) rs193922299
NM_000162.5(GCK):c.46-12C>T rs142829768
NM_000162.5(GCK):c.46-4438C>T
NM_000162.5(GCK):c.46-4952G>A
NM_000162.5(GCK):c.483+14A>G rs74852379
NM_000162.5(GCK):c.618G>A (p.Thr206=) rs142817246
NM_000162.5(GCK):c.645C>T (p.Tyr215=) rs144723656
NM_000162.5(GCK):c.660C>T (p.Cys220=) rs142952813
NM_000162.5(GCK):c.666C>T (p.Val222=) rs193922318
NM_000162.5(GCK):c.723G>A (p.Val241=) rs193922324
NM_000162.5(GCK):c.864-105G>A
NM_000162.5(GCK):c.954G>C (p.Gly318=) rs145764627
NM_000162.5(GCK):c.9C>T (p.Asp3=) rs142553382

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