ClinVar Miner

List of variants in gene GABRG2 studied for not provided

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Gene type:
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Total variants: 94
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HGVS dbSNP
GRCh37/hg19 5q34(chr5:161479977-161590162)x1
GRCh37/hg19 5q34(chr5:161555799-161624613)x1
NM_198903.2(GABRG2):c.-154C>T rs3219203
NM_198903.2(GABRG2):c.1005G>A (p.Trp335Ter) rs1554100509
NM_198903.2(GABRG2):c.1016A>T (p.Asp339Val) rs1554100510
NM_198903.2(GABRG2):c.1039T>G (p.Leu347Val) rs796052509
NM_198903.2(GABRG2):c.1042+108A>C
NM_198903.2(GABRG2):c.1042+6A>G rs375294947
NM_198903.2(GABRG2):c.1062A>G (p.Thr354=) rs377502016
NM_198903.2(GABRG2):c.1068C>A (p.Thr356=)
NM_198903.2(GABRG2):c.107+11C>A
NM_198903.2(GABRG2):c.107+223T>G
NM_198903.2(GABRG2):c.107+3A>G rs796052517
NM_198903.2(GABRG2):c.1074C>T (p.Leu358=) rs749531013
NM_198903.2(GABRG2):c.108-182G>A
NM_198903.2(GABRG2):c.1088G>A (p.Arg363Gln) rs397514737
NM_198903.2(GABRG2):c.1095G>A (p.Ser365=)
NM_198903.2(GABRG2):c.1120G>A (p.Ala374Thr) rs398123523
NM_198903.2(GABRG2):c.1149C>A (p.Phe383Leu) rs796052511
NM_198903.2(GABRG2):c.1149C>G (p.Phe383Leu) rs796052511
NM_198903.2(GABRG2):c.1207C>T (p.Arg403Trp) rs374512652
NM_198903.2(GABRG2):c.1208G>A (p.Arg403Gln) rs780199000
NM_198903.2(GABRG2):c.1230T>C (p.Asp410=) rs201824364
NM_198903.2(GABRG2):c.1232A>C (p.Lys411Thr) rs796052512
NM_198903.2(GABRG2):c.1233_1235del (p.Lys414del) rs727503941
NM_198903.2(GABRG2):c.1242A>G (p.Lys414=)
NM_198903.2(GABRG2):c.1248+99C>A
NM_198903.2(GABRG2):c.1248+9C>T
NM_198903.2(GABRG2):c.1273-7G>A
NM_198903.2(GABRG2):c.1273-8C>G
NM_198903.2(GABRG2):c.1276C>T (p.Pro426Ser) rs757311213
NM_198903.2(GABRG2):c.1290C>A (p.Ile430=)
NM_198903.2(GABRG2):c.1302A>G (p.Ser434=)
NM_198903.2(GABRG2):c.1337_1338del (p.Gln446fs) rs1554101202
NM_198903.2(GABRG2):c.1348G>T (p.Glu450Ter) rs1561662283
NM_198903.2(GABRG2):c.1356C>T (p.Tyr452=) rs749951528
NM_198903.2(GABRG2):c.1374C>T (p.Asp458=) rs113085352
NM_198903.2(GABRG2):c.13A>T (p.Asn5Tyr) rs774337016
NM_198903.2(GABRG2):c.1433G>A (p.Arg478Lys) rs796052514
NM_198903.2(GABRG2):c.1440G>A (p.Gly480=) rs150727562
NM_198903.2(GABRG2):c.1454G>T (p.Arg485Leu) rs587780341
NM_198903.2(GABRG2):c.1470C>T (p.Asp490=)
NM_198903.2(GABRG2):c.1480C>T (p.Arg494Trp) rs796052515
NM_198903.2(GABRG2):c.1518G>T (p.Leu506=)
NM_198903.2(GABRG2):c.220C>G (p.Leu74Val) rs796052503
NM_198903.2(GABRG2):c.243T>A (p.Leu81=) rs143295869
NM_198903.2(GABRG2):c.245G>A (p.Arg82Gln) rs121909673
NM_198903.2(GABRG2):c.247C>T (p.Pro83Ser) rs587777365
NM_198903.2(GABRG2):c.259+60A>T
NM_198903.2(GABRG2):c.260-9T>C
NM_198903.2(GABRG2):c.269C>T (p.Thr90Met) rs1057520498
NM_198903.2(GABRG2):c.272T>G (p.Leu91Ter) rs796052518
NM_198903.2(GABRG2):c.315C>T (p.Asn105=) rs11135176
NM_198903.2(GABRG2):c.316G>A (p.Ala106Thr) rs796052505
NM_198903.2(GABRG2):c.351dup (p.Ala118fs) rs1554097873
NM_198903.2(GABRG2):c.354G>A (p.Ala118=) rs61735412
NM_198903.2(GABRG2):c.360G>A (p.Thr120=) rs77298346
NM_198903.2(GABRG2):c.36A>T (p.Ser12=) rs762058667
NM_198903.2(GABRG2):c.409T>C (p.Leu137=) rs200828542
NM_198903.2(GABRG2):c.420C>T (p.Asn140=)
NM_198903.2(GABRG2):c.470A>C (p.Lys157Thr) rs770364855
NM_198903.2(GABRG2):c.471del (p.Ala158fs) rs1554097890
NM_198903.2(GABRG2):c.52G>C (p.Val18Leu)
NM_198903.2(GABRG2):c.540C>A (p.Tyr180Ter) rs1057520476
NM_198903.2(GABRG2):c.548+306C>T
NM_198903.2(GABRG2):c.549-3T>G rs750459631
NM_198903.2(GABRG2):c.571C>A (p.Gln191Lys) rs1334776746
NM_198903.2(GABRG2):c.582G>A (p.Leu194=) rs781498456
NM_198903.2(GABRG2):c.588C>T (p.Asn196=) rs211037
NM_198903.2(GABRG2):c.632-191C>T
NM_198903.2(GABRG2):c.643A>G (p.Ile215Val)
NM_198903.2(GABRG2):c.649C>T (p.Gln217Ter) rs886645578
NM_198903.2(GABRG2):c.703G>T (p.Gly235Cys)
NM_198903.2(GABRG2):c.70A>G (p.Thr24Ala) rs796052516
NM_198903.2(GABRG2):c.751+129C>T
NM_198903.2(GABRG2):c.751+52G>A
NM_198903.2(GABRG2):c.752-8C>T
NM_198903.2(GABRG2):c.790C>T (p.Arg264Ter) rs1045493304
NM_198903.2(GABRG2):c.810C>T (p.Gly270=)
NM_198903.2(GABRG2):c.811G>A (p.Asp271Asn) rs773065895
NM_198903.2(GABRG2):c.837A>G (p.Gln279=) rs78261481
NM_198903.2(GABRG2):c.868G>A (p.Glu290Lys) rs549251133
NM_198903.2(GABRG2):c.888C>T (p.Ser296=) rs201672465
NM_198903.2(GABRG2):c.890-1G>A rs796052507
NM_198903.2(GABRG2):c.890-230A>T
NM_198903.2(GABRG2):c.890-81A>G
NM_198903.2(GABRG2):c.918T>C (p.Phe306=) rs115126975
NM_198903.2(GABRG2):c.928A>C (p.Arg310=)
NM_198903.2(GABRG2):c.928A>G (p.Arg310Gly) rs796052520
NM_198903.2(GABRG2):c.942C>A (p.Tyr314Ter) rs1064794724
NM_198903.2(GABRG2):c.942C>G (p.Tyr314Ter) rs1064794724
NM_198903.2(GABRG2):c.964C>A (p.Pro322Thr) rs796052508
NM_198903.2(GABRG2):c.99C>T (p.Leu33=) rs368162707
NM_198903.2(GABRG2):c.9G>A (p.Ser3=)

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