ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 74
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HGVS dbSNP gnomAD frequency
NM_000162.5(GCK):c.363+317C>T rs145391098 0.02304
NM_000162.5(GCK):c.46-5701C>T rs73314180 0.01157
NM_000162.5(GCK):c.46-5702G>A rs150560724 0.00865
NM_000162.5(GCK):c.679+169C>T rs117031158 0.00775
NM_000162.5(GCK):c.864-105G>A rs139242745 0.00743
NM_000162.5(GCK):c.645C>T (p.Tyr215=) rs144723656 0.00682
NM_000162.5(GCK):c.46-4952G>A rs76178320 0.00639
NM_000162.5(GCK):c.46-5594A>G rs75119141 0.00607
NM_000162.5(GCK):c.339C>T (p.Asp113=) rs149412035 0.00451
NM_000162.5(GCK):c.618G>A (p.Thr206=) rs142817246 0.00400
NM_000162.5(GCK):c.1020-95G>A rs540085721 0.00397
NM_000162.5(GCK):c.*92C>A rs557990162 0.00389
NM_000162.5(GCK):c.46-4460G>T rs539644820 0.00387
NM_000162.5(GCK):c.46-4459C>T rs575328533 0.00384
NM_000162.5(GCK):c.1020-54G>A rs563914015 0.00323
NM_000162.5(GCK):c.1019+18G>A rs150914617 0.00322
NM_000162.5(GCK):c.46-62C>A rs191196720 0.00301
NM_000162.5(GCK):c.209-8G>A rs144798843 0.00249
NM_000162.5(GCK):c.660C>T (p.Cys220=) rs142952813 0.00109
NM_000162.5(GCK):c.46-5598A>T rs13306393 0.00046
NM_000162.5(GCK):c.208+17G>A rs199822205 0.00024
NM_000162.5(GCK):c.483+7C>T rs756053003 0.00024
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.364-13G>A rs372405219 0.00015
NM_000162.5(GCK):c.213C>T (p.Val71=) rs143128547 0.00014
NM_000162.5(GCK):c.1288C>T (p.Leu430=) rs193922276 0.00013
NM_000162.5(GCK):c.363+9C>T rs200985182 0.00011
NM_000162.5(GCK):c.9C>T (p.Asp3=) rs142553382 0.00009
NM_000162.5(GCK):c.483+8G>A rs151002306 0.00007
NM_000162.5(GCK):c.863+32C>A rs566348137 0.00007
NM_000162.5(GCK):c.561C>T (p.Asp187=) rs754722633 0.00006
NM_000162.5(GCK):c.600G>A (p.Val200=) rs773561406 0.00006
NM_000162.5(GCK):c.270G>A (p.Lys90=) rs571528578 0.00005
NM_000162.5(GCK):c.1068G>T (p.Gly356=) rs369103069 0.00004
NM_000162.5(GCK):c.363+6C>A rs751756042 0.00004
NM_000162.5(GCK):c.138G>A (p.Arg46=) rs550111033 0.00003
NM_000162.5(GCK):c.348C>T (p.Thr116=) rs770145567 0.00003
NM_000162.5(GCK):c.774C>T (p.Gly258=) rs780806456 0.00002
NM_000162.5(GCK):c.849C>T (p.Asn283=) rs199851776 0.00002
NM_000162.5(GCK):c.1248C>T (p.His416=) rs766653778 0.00001
NM_000162.5(GCK):c.609G>A (p.Val203=) rs776703291 0.00001
NM_000162.5(GCK):c.-217C>G rs73691419
NM_000162.5(GCK):c.-267G>T rs59914952
NM_000162.5(GCK):c.1020-7C>T
NM_000162.5(GCK):c.1137G>A (p.Ala379=)
NM_000162.5(GCK):c.1233C>G (p.Ser411=) rs755112715
NM_000162.5(GCK):c.1253+9G>A
NM_000162.5(GCK):c.1254-13C>G
NM_000162.5(GCK):c.1254-26G>A
NM_000162.5(GCK):c.1359G>T (p.Ser453=)
NM_000162.5(GCK):c.183C>T (p.Tyr61=) rs780612692
NM_000162.5(GCK):c.192C>T (p.Ser64=)
NM_000162.5(GCK):c.264G>A (p.Leu88=)
NM_000162.5(GCK):c.300C>T (p.Ser100=)
NM_000162.5(GCK):c.375C>T (p.Tyr125=)
NM_000162.5(GCK):c.432G>T (p.Leu144=)
NM_000162.5(GCK):c.46-4438C>A rs41282712
NM_000162.5(GCK):c.46-4438C>T rs41282712
NM_000162.5(GCK):c.46-4621C>T rs1562722328
NM_000162.5(GCK):c.46-4988G>C rs73314176
NM_000162.5(GCK):c.465G>A (p.Arg155=)
NM_000162.5(GCK):c.579+12C>G rs202001955
NM_000162.5(GCK):c.579+29G>T rs35786405
NM_000162.5(GCK):c.657G>A (p.Gln219=)
NM_000162.5(GCK):c.675C>A (p.Ile225=)
NM_000162.5(GCK):c.679+8C>G
NM_000162.5(GCK):c.680-14G>C rs577968084
NM_000162.5(GCK):c.680-19C>T
NM_000162.5(GCK):c.726G>A (p.Glu242=) rs373582283
NM_000162.5(GCK):c.835G>C (p.Glu279Gln) rs104894005
NM_000162.5(GCK):c.852C>G (p.Pro284=)
NM_000162.5(GCK):c.852C>T (p.Pro284=)
NM_000162.5(GCK):c.909G>T (p.Arg303=) rs1583594459

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