ClinVar Miner

List of variants in gene GRIN2B reported by Invitae

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Gene type:
ClinVar version:
Total variants: 138
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HGVS dbSNP
NM_000834.4(GRIN2B):c.1010+3G>A
NM_000834.4(GRIN2B):c.1023T>C (p.Asn341=) rs201228929
NM_000834.4(GRIN2B):c.1147T>G (p.Ser383Ala)
NM_000834.4(GRIN2B):c.1280G>T (p.Gly427Val)
NM_000834.4(GRIN2B):c.1287C>T (p.Cys429=)
NM_000834.4(GRIN2B):c.1338A>G (p.Thr446=) rs141031272
NM_000834.4(GRIN2B):c.1341C>T (p.Asp447=) rs35025065
NM_000834.4(GRIN2B):c.1345G>T (p.Glu449Ter) rs1555112186
NM_000834.4(GRIN2B):c.138C>T (p.Asp46=) rs200527066
NM_000834.4(GRIN2B):c.140A>G (p.Glu47Gly) rs199526748
NM_000834.4(GRIN2B):c.144G>A (p.Val48=) rs201242152
NM_000834.4(GRIN2B):c.1547A>G (p.Asn516Ser) rs886041295
NM_000834.4(GRIN2B):c.1704C>T (p.Ile568=) rs202102041
NM_000834.4(GRIN2B):c.1705G>A (p.Val569Ile) rs1293991066
NM_000834.4(GRIN2B):c.174T>C (p.Asp58=) rs1555149549
NM_000834.4(GRIN2B):c.1780+8C>T rs199986080
NM_000834.4(GRIN2B):c.1781-3C>T
NM_000834.4(GRIN2B):c.1821G>A (p.Trp607Ter)
NM_000834.4(GRIN2B):c.1851C>T (p.Ser617=) rs147373250
NM_000834.4(GRIN2B):c.1878C>A (p.Thr626=) rs1555110827
NM_000834.4(GRIN2B):c.190G>A (p.Val64Met) rs150070901
NM_000834.4(GRIN2B):c.2002G>A (p.Asp668Asn) rs876661151
NM_000834.4(GRIN2B):c.2017A>C (p.Arg673=) rs149279923
NM_000834.4(GRIN2B):c.2053A>C (p.Thr685Pro) rs869312669
NM_000834.4(GRIN2B):c.2064C>A (p.Asn688Lys)
NM_000834.4(GRIN2B):c.2078G>C (p.Arg693Thr) rs1565457884
NM_000834.4(GRIN2B):c.2087G>A (p.Arg696His) rs1555103971
NM_000834.4(GRIN2B):c.2099C>G (p.Ala700Gly) rs1191539298
NM_000834.4(GRIN2B):c.2125T>G (p.Phe709Val)
NM_000834.4(GRIN2B):c.2172-10delT rs761900678
NM_000834.4(GRIN2B):c.2172-6G>A rs201390691
NM_000834.4(GRIN2B):c.2172-8C>T rs751592819
NM_000834.4(GRIN2B):c.2177T>C (p.Leu726Pro)
NM_000834.4(GRIN2B):c.2202A>G (p.Ala734=) rs148185805
NM_000834.4(GRIN2B):c.2247G>A (p.Val749=) rs757990373
NM_000834.4(GRIN2B):c.228C>T (p.Thr76=) rs77299791
NM_000834.4(GRIN2B):c.23G>C (p.Cys8Ser) rs1060503160
NM_000834.4(GRIN2B):c.2453T>G (p.Met818Arg) rs879254016
NM_000834.4(GRIN2B):c.2459G>A (p.Gly820Glu)
NM_000834.4(GRIN2B):c.2459G>C (p.Gly820Ala) rs797044849
NM_000834.4(GRIN2B):c.2481G>A (p.Ala827=) rs189384622
NM_000834.4(GRIN2B):c.2510T>C (p.Ile837Thr) rs1565455844
NM_000834.4(GRIN2B):c.2539C>T (p.Arg847Ter) rs879253931
NM_000834.4(GRIN2B):c.2540G>A (p.Arg847Gln)
NM_000834.4(GRIN2B):c.2561G>T (p.Cys854Phe)
NM_000834.4(GRIN2B):c.2662A>G (p.Thr888Ala) rs200256539
NM_000834.4(GRIN2B):c.2691C>T (p.Asn897=) rs35125534
NM_000834.4(GRIN2B):c.2703G>A (p.Leu901=) rs145005918
NM_000834.4(GRIN2B):c.2715C>T (p.Ala905=) rs568858172
NM_000834.4(GRIN2B):c.2741T>C (p.Val914Ala) rs1565454741
NM_000834.4(GRIN2B):c.2754G>A (p.Pro918=) rs756487785
NM_000834.4(GRIN2B):c.2813G>A (p.Arg938His) rs150445188
NM_000834.4(GRIN2B):c.2847C>T (p.Tyr949=) rs771565713
NM_000834.4(GRIN2B):c.2854C>T (p.Pro952Ser) rs1565454641
NM_000834.4(GRIN2B):c.2913G>A (p.Gly971=) rs200696950
NM_000834.4(GRIN2B):c.291G>A (p.Val97=) rs202223470
NM_000834.4(GRIN2B):c.2931C>G (p.Asp977Glu) rs147956755
NM_000834.4(GRIN2B):c.2936A>T (p.Asn979Ile) rs796052574
NM_000834.4(GRIN2B):c.2960A>G (p.His987Arg) rs765183831
NM_000834.4(GRIN2B):c.2975A>G (p.His992Arg) rs1555102461
NM_000834.4(GRIN2B):c.3028C>T (p.Pro1010Ser)
NM_000834.4(GRIN2B):c.3043T>G (p.Ser1015Ala)
NM_000834.4(GRIN2B):c.3047G>A (p.Arg1016Lys) rs141109968
NM_000834.4(GRIN2B):c.3076G>A (p.Gly1026Ser) rs201963596
NM_000834.4(GRIN2B):c.3078C>T (p.Gly1026=) rs1555102406
NM_000834.4(GRIN2B):c.3085_3087TCC[1] (p.Ser1030del) rs878854145
NM_000834.4(GRIN2B):c.3102G>C (p.Gln1034His)
NM_000834.4(GRIN2B):c.3117C>T (p.Tyr1039=) rs147762014
NM_000834.4(GRIN2B):c.3118G>A (p.Gly1040Ser) rs202222002
NM_000834.4(GRIN2B):c.3146A>G (p.Tyr1049Cys) rs201866998
NM_000834.4(GRIN2B):c.3174C>T (p.Ser1058=) rs772364390
NM_000834.4(GRIN2B):c.3202G>A (p.Val1068Ile)
NM_000834.4(GRIN2B):c.3275G>A (p.Arg1092Gln) rs1555102321
NM_000834.4(GRIN2B):c.3285G>A (p.Ser1095=) rs200058641
NM_000834.4(GRIN2B):c.3306T>C (p.Phe1102=) rs763445499
NM_000834.4(GRIN2B):c.3332G>A (p.Arg1111His) rs876661167
NM_000834.4(GRIN2B):c.3339G>A (p.Pro1113=) rs200660626
NM_000834.4(GRIN2B):c.3367T>C (p.Phe1123Leu)
NM_000834.4(GRIN2B):c.336C>T (p.Leu112=) rs1060504845
NM_000834.4(GRIN2B):c.3389G>A (p.Arg1130Gln) rs148625092
NM_000834.4(GRIN2B):c.3400C>G (p.Leu1134Val)
NM_000834.4(GRIN2B):c.3409T>A (p.Phe1137Ile) rs1060503159
NM_000834.4(GRIN2B):c.3415A>G (p.Thr1139Ala)
NM_000834.4(GRIN2B):c.3473G>C (p.Arg1158Pro)
NM_000834.4(GRIN2B):c.3493G>A (p.Asp1165Asn) rs769857006
NM_000834.4(GRIN2B):c.3498C>T (p.Ser1166=) rs45600931
NM_000834.4(GRIN2B):c.3505G>A (p.Gly1169Arg) rs777639067
NM_000834.4(GRIN2B):c.3552C>T (p.Gly1184=) rs141886903
NM_000834.4(GRIN2B):c.3648C>T (p.Arg1216=) rs201405157
NM_000834.4(GRIN2B):c.3683C>T (p.Thr1228Met) rs75670883
NM_000834.4(GRIN2B):c.3747C>T (p.Gly1249=) rs138771137
NM_000834.4(GRIN2B):c.3799G>T (p.Ala1267Ser) rs141844705
NM_000834.4(GRIN2B):c.3807A>G (p.Pro1269=) rs78765966
NM_000834.4(GRIN2B):c.3807A>T (p.Pro1269=) rs78765966
NM_000834.4(GRIN2B):c.3837T>G (p.Thr1279=) rs1806200
NM_000834.4(GRIN2B):c.3838A>G (p.Lys1280Glu)
NM_000834.4(GRIN2B):c.3886A>C (p.Asn1296His) rs1555101871
NM_000834.4(GRIN2B):c.3922G>A (p.Val1308Met) rs374746622
NM_000834.4(GRIN2B):c.3944C>T (p.Ala1315Val)
NM_000834.4(GRIN2B):c.3946G>A (p.Ala1316Thr) rs199803550
NM_000834.4(GRIN2B):c.3957G>A (p.Pro1319=) rs141730031
NM_000834.4(GRIN2B):c.3964G>C (p.Val1322Leu) rs200255226
NM_000834.4(GRIN2B):c.3981G>A (p.Lys1327=) rs201670483
NM_000834.4(GRIN2B):c.3993G>A (p.Met1331Ile) rs200035225
NM_000834.4(GRIN2B):c.4041C>A (p.Ser1347Arg) rs769147604
NM_000834.4(GRIN2B):c.4105G>A (p.Gly1369Ser) rs371190262
NM_000834.4(GRIN2B):c.4113C>T (p.Tyr1371=) rs146792012
NM_000834.4(GRIN2B):c.4196A>G (p.His1399Arg) rs1565452791
NM_000834.4(GRIN2B):c.4218C>T (p.Phe1406=) rs1805246
NM_000834.4(GRIN2B):c.4229C>T (p.Thr1410Met)
NM_000834.4(GRIN2B):c.4230G>A (p.Thr1410=) rs149655315
NM_000834.4(GRIN2B):c.4240G>T (p.Ala1414Ser) rs140744818
NM_000834.4(GRIN2B):c.4270C>T (p.Leu1424Phe)
NM_000834.4(GRIN2B):c.4296G>A (p.Ser1432=) rs755880051
NM_000834.4(GRIN2B):c.4307G>C (p.Gly1436Ala) rs1565452616
NM_000834.4(GRIN2B):c.4322G>A (p.Arg1441His) rs200903876
NM_000834.4(GRIN2B):c.4326C>G (p.Phe1442Leu) rs1565452565
NM_000834.4(GRIN2B):c.4416T>G (p.His1472Gln) rs1555101497
NM_000834.4(GRIN2B):c.4432T>C (p.Ser1478Pro)
NM_000834.4(GRIN2B):c.45G>A (p.Val15=) rs374735893
NM_000834.4(GRIN2B):c.465C>A (p.Ser155=) rs115189840
NM_000834.4(GRIN2B):c.504C>A (p.Ile168=) rs36031537
NM_000834.4(GRIN2B):c.513C>T (p.Ile171=) rs3026183
NM_000834.4(GRIN2B):c.514G>A (p.Val172Ile) rs201377003
NM_000834.4(GRIN2B):c.519C>G (p.Thr173=) rs200357530
NM_000834.4(GRIN2B):c.542A>G (p.Asp181Gly) rs1060503161
NM_000834.4(GRIN2B):c.61G>A (p.Val21Met) rs79046967
NM_000834.4(GRIN2B):c.674G>A (p.Ser225Asn) rs1060503158
NM_000834.4(GRIN2B):c.679A>G (p.Ile227Val) rs201672517
NM_000834.4(GRIN2B):c.681C>A (p.Ile227=) rs148254591
NM_000834.4(GRIN2B):c.732C>G (p.Ala244=) rs201554036
NM_000834.4(GRIN2B):c.765G>A (p.Thr255=) rs199844735
NM_000834.4(GRIN2B):c.771C>T (p.Ile257=) rs142203984
NM_000834.4(GRIN2B):c.870C>T (p.Pro290=) rs1124894
NM_000834.4(GRIN2B):c.923T>C (p.Leu308Pro) rs1565524674
NM_000834.4(GRIN2B):c.92G>C (p.Ser31Thr)
NM_000834.4(GRIN2B):c.975C>T (p.His325=) rs200380868
NM_000834.4(GRIN2B):c.992A>G (p.Gln331Arg)

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