ClinVar Miner

List of variants in gene GNB3 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 113
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HGVS dbSNP gnomAD frequency
NM_002075.4(GNB3):c.699+115del rs1482567541 0.03114
NM_002075.4(GNB3):c.96+16C>G rs371123230 0.00081
NM_002075.4(GNB3):c.147G>A (p.Arg49=) rs376832139 0.00024
NM_002075.4(GNB3):c.58-19A>G rs367711032 0.00021
NM_002075.4(GNB3):c.96+15C>T rs782160261 0.00016
NM_002075.4(GNB3):c.192C>T (p.Ala64=) rs1375864982 0.00015
NM_002075.4(GNB3):c.96+11C>T rs782762128 0.00014
NM_002075.4(GNB3):c.177C>T (p.Tyr59=) rs146702158 0.00012
NM_002075.4(GNB3):c.431-9C>T rs377593669 0.00010
NM_002075.4(GNB3):c.33G>A (p.Ala11=) rs566098814 0.00009
NM_002075.4(GNB3):c.495G>A (p.Thr165=) rs781817983 0.00008
NM_002075.4(GNB3):c.203+20C>T rs781784104 0.00005
NM_002075.4(GNB3):c.204-18G>A rs781840504 0.00005
NM_002075.4(GNB3):c.240C>T (p.Ile80=) rs190325696 0.00005
NM_002075.4(GNB3):c.249C>T (p.Asp83=) rs782395053 0.00005
NM_002075.4(GNB3):c.504G>A (p.Leu168=) rs138319468 0.00005
NM_002075.4(GNB3):c.621T>C (p.Ser207=) rs373970960 0.00005
NM_002075.4(GNB3):c.699+113_699+115del rs1943631887 0.00005
NM_002075.4(GNB3):c.447C>T (p.Cys149=) rs368740450 0.00004
NM_002075.4(GNB3):c.498-14C>T rs782615277 0.00004
NM_002075.4(GNB3):c.681G>A (p.Ser227=) rs374134015 0.00004
NM_002075.4(GNB3):c.96+19C>T rs781874487 0.00004
NM_002075.4(GNB3):c.273C>T (p.His91=) rs781925945 0.00003
NM_002075.4(GNB3):c.285G>A (p.Leu95=) rs782251534 0.00003
NM_002075.4(GNB3):c.58-9T>C rs13306408 0.00003
NM_002075.4(GNB3):c.96+20G>A rs782112871 0.00003
NM_002075.4(GNB3):c.97-16G>A rs782532802 0.00003
NM_002075.4(GNB3):c.203+9T>G rs1418141070 0.00002
NM_002075.4(GNB3):c.222G>A (p.Ser74=) rs1943608495 0.00002
NM_002075.4(GNB3):c.483G>A (p.Ser161=) rs75977062 0.00002
NM_002075.4(GNB3):c.498-11C>T rs201972812 0.00002
NM_002075.4(GNB3):c.567C>T (p.Ser189=) rs781903842 0.00002
NM_002075.4(GNB3):c.690C>T (p.Asn230=) rs367720671 0.00002
NM_002075.4(GNB3):c.97-11T>C rs1555123684 0.00002
NM_002075.4(GNB3):c.150G>A (p.Thr50=) rs1382910777 0.00001
NM_002075.4(GNB3):c.204-19T>A rs782759905 0.00001
NM_002075.4(GNB3):c.267+12G>C rs781935145 0.00001
NM_002075.4(GNB3):c.268-6C>T rs1555123809 0.00001
NM_002075.4(GNB3):c.306C>T (p.Thr102=) rs200048512 0.00001
NM_002075.4(GNB3):c.430+15C>T rs28395777 0.00001
NM_002075.4(GNB3):c.431-8G>A rs782568174 0.00001
NM_002075.4(GNB3):c.497+19G>C rs1943621367 0.00001
NM_002075.4(GNB3):c.498-12C>T rs782199199 0.00001
NM_002075.4(GNB3):c.558C>T (p.Asp186=) rs139141966 0.00001
NM_002075.4(GNB3):c.57+14C>T rs892715161 0.00001
NM_002075.4(GNB3):c.675C>T (p.His225=) rs1465671356 0.00001
NM_002075.4(GNB3):c.684C>T (p.Asp228=) rs1943628549 0.00001
NM_002075.4(GNB3):c.96+12del rs782129332 0.00001
NM_002075.4(GNB3):c.129C>T (p.Val43=) rs2137981458
NM_002075.4(GNB3):c.203+10G>T rs782363697
NM_002075.4(GNB3):c.203+11G>A rs373777248
NM_002075.4(GNB3):c.203+11G>T rs373777248
NM_002075.4(GNB3):c.203+12G>A rs377392819
NM_002075.4(GNB3):c.203+12G>C rs377392819
NM_002075.4(GNB3):c.203+12G>T
NM_002075.4(GNB3):c.203+14_203+16del rs545677946
NM_002075.4(GNB3):c.203+16dup rs545677946
NM_002075.4(GNB3):c.203+20C>A rs781784104
NM_002075.4(GNB3):c.228T>C (p.Asp76=)
NM_002075.4(GNB3):c.264C>T (p.Asn88=) rs1365142672
NM_002075.4(GNB3):c.267+18C>A rs1943610295
NM_002075.4(GNB3):c.267+8C>A rs371433292
NM_002075.4(GNB3):c.267+8C>T rs371433292
NM_002075.4(GNB3):c.268-14C>T
NM_002075.4(GNB3):c.270G>A (p.Val90=) rs2542349694
NM_002075.4(GNB3):c.282A>G (p.Pro94=) rs1943613040
NM_002075.4(GNB3):c.283C>T (p.Leu95=) rs1943613079
NM_002075.4(GNB3):c.315T>C (p.Tyr105=) rs2137983225
NM_002075.4(GNB3):c.33G>T (p.Ala11=) rs566098814
NM_002075.4(GNB3):c.366C>G (p.Ser122=) rs2137983404
NM_002075.4(GNB3):c.369C>A (p.Ile123=) rs2542350192
NM_002075.4(GNB3):c.390G>A (p.Glu130=)
NM_002075.4(GNB3):c.39G>A (p.Gln13=) rs2137976501
NM_002075.4(GNB3):c.414G>A (p.Glu138=) rs782343782
NM_002075.4(GNB3):c.430+19C>A rs1819707575
NM_002075.4(GNB3):c.456G>A (p.Leu152=) rs781988924
NM_002075.4(GNB3):c.459T>C (p.Asp153=) rs200864177
NM_002075.4(GNB3):c.45G>A (p.Lys15=) rs2542343177
NM_002075.4(GNB3):c.474G>A (p.Val158=)
NM_002075.4(GNB3):c.497+7C>G rs2542351190
NM_002075.4(GNB3):c.498-12C>G rs782199199
NM_002075.4(GNB3):c.498-16C>A rs1943622899
NM_002075.4(GNB3):c.498-35_498-14del rs2542351339
NM_002075.4(GNB3):c.552G>A (p.Thr184=) rs1943624936
NM_002075.4(GNB3):c.57+19C>T rs1555123332
NM_002075.4(GNB3):c.57+8_57+10del
NM_002075.4(GNB3):c.676G>C (p.Glu226Gln) rs371744474
NM_002075.4(GNB3):c.699+114_699+115insC rs1555124071
NM_002075.4(GNB3):c.699+114_699+115insCT
NM_002075.4(GNB3):c.699+115A>G rs11064426
NM_002075.4(GNB3):c.699+115A>T rs11064426
NM_002075.4(GNB3):c.699+115_699+116del rs1357316889
NM_002075.4(GNB3):c.699+115_699+117del rs2137986155
NM_002075.4(GNB3):c.699+115_699+118del rs1943632632
NM_002075.4(GNB3):c.699+115_699+119del rs1171910840
NM_002075.4(GNB3):c.699+115_699+120del rs1449478569
NM_002075.4(GNB3):c.699+115_699+121del rs1943632765
NM_002075.4(GNB3):c.699+115_699+122del rs1943632804
NM_002075.4(GNB3):c.699+115_699+123del rs1389229148
NM_002075.4(GNB3):c.699+115_699+124del rs1186271758
NM_002075.4(GNB3):c.699+115_699+125del
NM_002075.4(GNB3):c.699+115_699+126del rs1446862970
NM_002075.4(GNB3):c.699+115_699+127del rs1257270384
NM_002075.4(GNB3):c.699+115_699+128del rs1181586303
NM_002075.4(GNB3):c.699+129_699+141del rs34871066
NM_002075.4(GNB3):c.699+12C>T rs2542352730
NM_002075.4(GNB3):c.699+133_699+141del rs34871066
NM_002075.4(GNB3):c.699+140_699+141dup rs34871066
NM_002075.4(GNB3):c.699+15C>A rs781906487
NM_002075.4(GNB3):c.699+15C>G
NM_002075.4(GNB3):c.699+15C>T rs781906487
NM_002075.4(GNB3):c.97-15C>T rs2542347748
NM_002075.4(GNB3):c.97-9T>C rs2137981273

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