ClinVar Miner

List of variants in gene GCK reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_000162.5(GCK):c.1253+8C>T rs2908274 0.34109
NM_000162.5(GCK):c.645C>T (p.Tyr215=) rs144723656 0.00682
NM_000162.5(GCK):c.31G>A (p.Ala11Thr) rs116093166 0.00663
NM_000162.5(GCK):c.339C>T (p.Asp113=) rs149412035 0.00451
NM_000162.5(GCK):c.46-12C>T rs142829768 0.00296
NM_000162.5(GCK):c.954G>C (p.Gly318=) rs145764627 0.00287
NM_000162.5(GCK):c.209-8G>A rs144798843 0.00249
NM_000162.5(GCK):c.333C>T (p.Pro111=) rs61736250 0.00235
NM_000162.5(GCK):c.-455A>G rs140894490 0.00101
NM_000162.5(GCK):c.483+26C>A rs142668032 0.00048
NM_000162.5(GCK):c.*11C>T rs200698755 0.00046
NM_000162.5(GCK):c.483+8G>A rs151002306 0.00007
NM_000162.5(GCK):c.600G>A (p.Val200=) rs773561406 0.00006
NM_000162.5(GCK):c.834C>T (p.Asp278=) rs200071687 0.00004
NM_000162.5(GCK):c.138G>A (p.Arg46=) rs550111033 0.00003
NM_000162.5(GCK):c.129C>T (p.Arg43=) rs760912915 0.00001
NM_000162.5(GCK):c.370G>A (p.Asp124Asn) rs759072800 0.00001
NM_000162.5(GCK):c.609G>A (p.Val203=) rs776703291 0.00001
NM_000162.3(GCK):c.-557G>C
NM_000162.5(GCK):c.-450C>T
NM_000162.5(GCK):c.1014G>A (p.Val338=)
NM_000162.5(GCK):c.1020-8C>T
NM_000162.5(GCK):c.1106G>C (p.Arg369Pro)
NM_000162.5(GCK):c.1151C>T (p.Ala384Val) rs1583591747
NM_000162.5(GCK):c.1174C>G (p.Arg392Gly) rs1167124132
NM_000162.5(GCK):c.1174C>T (p.Arg392Cys) rs1167124132
NM_000162.5(GCK):c.1183_1209del (p.Glu395_Arg403del)
NM_000162.5(GCK):c.1233C>G (p.Ser411=) rs755112715
NM_000162.5(GCK):c.1240A>G (p.Lys414Glu) rs193922272
NM_000162.5(GCK):c.1253+1G>A
NM_000162.5(GCK):c.1255T>C (p.Phe419Leu) rs1554334478
NM_000162.5(GCK):c.1265G>T (p.Arg422Leu)
NM_000162.5(GCK):c.1270C>T (p.His424Tyr)
NM_000162.5(GCK):c.128G>A (p.Arg43His) rs764232985
NM_000162.5(GCK):c.130G>T (p.Gly44Cys)
NM_000162.5(GCK):c.1322C>G (p.Ser441Trp) rs1286804191
NM_000162.5(GCK):c.219C>G (p.Asp73Glu)
NM_000162.5(GCK):c.292C>T (p.Gln98Ter)
NM_000162.5(GCK):c.364-1G>C
NM_000162.5(GCK):c.369C>T (p.Phe123=)
NM_000162.5(GCK):c.373T>A (p.Tyr125Asn)
NM_000162.5(GCK):c.46-11T>A
NM_000162.5(GCK):c.46-14C>A
NM_000162.5(GCK):c.46-4647C>A
NM_000162.5(GCK):c.468C>T (p.His156=)
NM_000162.5(GCK):c.521C>T (p.Ser174Leu)
NM_000162.5(GCK):c.527C>A (p.Ala176Glu) rs193922304
NM_000162.5(GCK):c.566T>C (p.Ile189Thr) rs1554335441
NM_000162.5(GCK):c.765C>T (p.Thr255=)
NM_000162.5(GCK):c.786del (p.Ser263fs)
NM_000162.5(GCK):c.859C>G (p.Gln287Glu)

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