ClinVar Miner

List of variants in gene GRIN2B reported as benign for Intellectual disability, autosomal dominant 6; Developmental and epileptic encephalopathy, 27

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Gene type:
ClinVar version:
Total variants: 184
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HGVS dbSNP gnomAD frequency
NM_000834.5(GRIN2B):c.366C>G (p.Pro122=) rs7301328 0.41972
NM_000834.5(GRIN2B):c.3534C>T (p.His1178=) rs1806191 0.39095
NM_000834.5(GRIN2B):c.1665C>T (p.Ser555=) rs1805482 0.26553
NM_000834.5(GRIN2B):c.2664C>T (p.Thr888=) rs1806201 0.23527
NM_000834.5(GRIN2B):c.4197T>C (p.His1399=) rs1805247 0.16667
NM_000834.5(GRIN2B):c.1125+20A>G rs11055581 0.14832
NM_000834.5(GRIN2B):c.2514C>T (p.Cys838=) rs3026160 0.08178
NM_000834.5(GRIN2B):c.1126-12A>G rs76777620 0.03782
NM_000834.5(GRIN2B):c.15G>A (p.Ala5=) rs34315573 0.03193
NM_000834.5(GRIN2B):c.870C>T (p.Pro290=) rs1124894 0.02647
NM_000834.5(GRIN2B):c.4218C>T (p.Phe1406=) rs1805246 0.02603
NM_000834.5(GRIN2B):c.504C>A (p.Ile168=) rs36031537 0.01733
NM_000834.5(GRIN2B):c.2691C>T (p.Asn897=) rs35125534 0.01112
NM_000834.5(GRIN2B):c.1341C>T (p.Asp447=) rs35025065 0.00902
NM_000834.5(GRIN2B):c.3498C>T (p.Ser1166=) rs45600931 0.00538
NM_000834.5(GRIN2B):c.3552C>T (p.Gly1184=) rs141886903 0.00206
NM_000834.5(GRIN2B):c.3117C>T (p.Tyr1039=) rs147762014 0.00123
NM_000834.5(GRIN2B):c.1338A>G (p.Thr446=) rs141031272 0.00102
NM_000834.5(GRIN2B):c.1569C>T (p.Val523=) rs148573953 0.00081
NM_000834.5(GRIN2B):c.228C>T (p.Thr76=) rs77299791 0.00070
NM_000834.5(GRIN2B):c.1780+8C>T rs199986080 0.00068
NM_000834.5(GRIN2B):c.3747C>T (p.Gly1249=) rs138771137 0.00063
NM_000834.5(GRIN2B):c.1851C>T (p.Ser617=) rs147373250 0.00045
NM_000834.5(GRIN2B):c.4101C>T (p.Pro1367=) rs112932810 0.00043
NM_000834.5(GRIN2B):c.4230G>A (p.Thr1410=) rs149655315 0.00041
NM_000834.5(GRIN2B):c.45G>A (p.Val15=) rs374735893 0.00030
NM_000834.5(GRIN2B):c.3799G>T (p.Ala1267Ser) rs141844705 0.00029
NM_000834.5(GRIN2B):c.4113C>T (p.Tyr1371=) rs146792012 0.00029
NM_000834.5(GRIN2B):c.2703G>A (p.Leu901=) rs145005918 0.00026
NM_000834.5(GRIN2B):c.1780+9G>A rs201461091 0.00017
NM_000834.5(GRIN2B):c.2599-19C>A rs3751258 0.00017
NM_000834.5(GRIN2B):c.1328+17A>G rs201560542 0.00011
NM_000834.5(GRIN2B):c.190G>A (p.Val64Met) rs150070901 0.00011
NM_000834.5(GRIN2B):c.3076G>A (p.Gly1026Ser) rs201963596 0.00011
NM_000834.5(GRIN2B):c.1781-3C>T rs201520798 0.00010
NM_000834.5(GRIN2B):c.771C>T (p.Ile257=) rs142203984 0.00010
NM_000834.5(GRIN2B):c.140A>G (p.Glu47Gly) rs199526748 0.00008
NM_000834.5(GRIN2B):c.2628G>A (p.Ala876=) rs199710029 0.00007
NM_000834.5(GRIN2B):c.1768G>A (p.Ala590Thr) rs145021339 0.00006
NM_000834.5(GRIN2B):c.270T>C (p.Ser90=) rs540429850 0.00006
NM_000834.5(GRIN2B):c.3047G>A (p.Arg1016Lys) rs141109968 0.00006
NM_000834.5(GRIN2B):c.3797C>T (p.Pro1266Leu) rs201947553 0.00006
NM_000834.5(GRIN2B):c.3818C>A (p.Thr1273Lys) rs531747728 0.00006
NM_000834.5(GRIN2B):c.4270C>T (p.Leu1424Phe) rs748128078 0.00006
NM_000834.5(GRIN2B):c.3473G>A (p.Arg1158Gln) rs143955920 0.00005
NM_000834.5(GRIN2B):c.412-20T>C rs779719544 0.00005
NM_000834.5(GRIN2B):c.2648T>C (p.Val883Ala) rs770464893 0.00004
NM_000834.5(GRIN2B):c.275G>A (p.Arg92Gln) rs201966022 0.00004
NM_000834.5(GRIN2B):c.3993G>A (p.Met1331Ile) rs200035225 0.00004
NM_000834.5(GRIN2B):c.4041C>A (p.Ser1347Arg) rs769147604 0.00004
NM_000834.5(GRIN2B):c.2845T>C (p.Tyr949His) rs201982602 0.00003
NM_000834.5(GRIN2B):c.2861G>A (p.Cys954Tyr) rs376328340 0.00003
NM_000834.5(GRIN2B):c.3837T>G (p.Thr1279=) rs1806200 0.00003
NM_000834.5(GRIN2B):c.4107C>T (p.Gly1369=) rs201732760 0.00003
NM_000834.5(GRIN2B):c.4321C>T (p.Arg1441Cys) rs773648473 0.00003
NM_000834.5(GRIN2B):c.2172-9C>G rs1555103671 0.00002
NM_000834.5(GRIN2B):c.3338C>T (p.Pro1113Leu) rs766946947 0.00002
NM_000834.5(GRIN2B):c.3499G>A (p.Val1167Ile) rs1042339 0.00002
NM_000834.5(GRIN2B):c.3514C>T (p.Pro1172Ser) rs757924519 0.00002
NM_000834.5(GRIN2B):c.3884G>A (p.Arg1295Gln) rs1284336148 0.00002
NM_000834.5(GRIN2B):c.4105G>A (p.Gly1369Ser) rs371190262 0.00002
NM_000834.5(GRIN2B):c.52G>A (p.Val18Ile) rs201094029 0.00002
NM_000834.5(GRIN2B):c.598G>C (p.Glu200Gln) rs1196117849 0.00002
NM_000834.5(GRIN2B):c.1010+3G>A rs771246986 0.00001
NM_000834.5(GRIN2B):c.1125+9T>C rs764590430 0.00001
NM_000834.5(GRIN2B):c.1318A>G (p.Ile440Val) rs765062440 0.00001
NM_000834.5(GRIN2B):c.14C>T (p.Ala5Val) rs367543147 0.00001
NM_000834.5(GRIN2B):c.2325G>C (p.Gln775His) rs774981179 0.00001
NM_000834.5(GRIN2B):c.2627C>T (p.Ala876Val) rs1458368988 0.00001
NM_000834.5(GRIN2B):c.2700C>A (p.Arg900=) rs531269037 0.00001
NM_000834.5(GRIN2B):c.2938G>A (p.Val980Met) rs778202551 0.00001
NM_000834.5(GRIN2B):c.3049T>G (p.Ser1017Ala) rs1948601205 0.00001
NM_000834.5(GRIN2B):c.3148A>G (p.Ser1050Gly) rs1157190922 0.00001
NM_000834.5(GRIN2B):c.3170G>A (p.Arg1057His) rs773737239 0.00001
NM_000834.5(GRIN2B):c.3402G>A (p.Leu1134=) rs1227988479 0.00001
NM_000834.5(GRIN2B):c.3588T>C (p.Pro1196=) rs200884387 0.00001
NM_000834.5(GRIN2B):c.3660C>G (p.Ser1220=) rs201983807 0.00001
NM_000834.5(GRIN2B):c.3683C>T (p.Thr1228Met) rs75670883 0.00001
NM_000834.5(GRIN2B):c.3685G>A (p.Val1229Met) rs1948582128 0.00001
NM_000834.5(GRIN2B):c.3805C>T (p.Pro1269Ser) rs1458120181 0.00001
NM_000834.5(GRIN2B):c.4035C>T (p.Gly1345=) rs776247380 0.00001
NM_000834.5(GRIN2B):c.4049C>T (p.Ala1350Val) rs763372245 0.00001
NM_000834.5(GRIN2B):c.4093A>C (p.Asn1365His) rs1330186615 0.00001
NM_000834.5(GRIN2B):c.4102G>A (p.Gly1368Ser) rs1043559346 0.00001
NM_000834.5(GRIN2B):c.4112A>G (p.Tyr1371Cys) rs755797497 0.00001
NM_000834.5(GRIN2B):c.4148C>T (p.Thr1383Met) rs775838374 0.00001
NM_000834.5(GRIN2B):c.4205A>G (p.Lys1402Arg) rs1349506481 0.00001
NM_000834.5(GRIN2B):c.4229C>T (p.Thr1410Met) rs779830552 0.00001
NM_000834.5(GRIN2B):c.4235C>A (p.Ala1412Glu) rs1314346300 0.00001
NM_000834.5(GRIN2B):c.4244C>T (p.Ser1415Leu) rs201463390 0.00001
NM_000834.5(GRIN2B):c.425T>C (p.Met142Thr) rs1184168879 0.00001
NM_000834.5(GRIN2B):c.4265G>A (p.Arg1422Gln) rs75269586 0.00001
NM_000834.5(GRIN2B):c.4286C>T (p.Pro1429Leu) rs1261054497 0.00001
NM_000834.5(GRIN2B):c.4322G>A (p.Arg1441His) rs200903876 0.00001
NM_000834.5(GRIN2B):c.4355C>T (p.Ser1452Phe) rs756790727 0.00001
NM_000834.5(GRIN2B):c.4375A>G (p.Asn1459Asp) rs1384338205 0.00001
NM_000834.5(GRIN2B):c.568A>G (p.Ile190Val) rs1863531293 0.00001
NM_000834.5(GRIN2B):c.619A>G (p.Met207Val) rs747790101 0.00001
NM_000834.5(GRIN2B):c.679A>G (p.Ile227Val) rs201672517 0.00001
NM_000834.5(GRIN2B):c.871G>A (p.Ala291Thr) rs1246772896 0.00001
NM_000834.5(GRIN2B):c.998A>G (p.Asn333Ser) rs748965398 0.00001
NM_000834.5(GRIN2B):c.104T>C (p.Ile35Thr) rs201568626
NM_000834.5(GRIN2B):c.1103A>C (p.Asn368Thr) rs1314805334
NM_000834.5(GRIN2B):c.1146G>C (p.Lys382Asn)
NM_000834.5(GRIN2B):c.1147T>A (p.Ser383Thr) rs199671864
NM_000834.5(GRIN2B):c.1288A>C (p.Met430Leu)
NM_000834.5(GRIN2B):c.1479C>G (p.Thr493=) rs202139349
NM_000834.5(GRIN2B):c.163G>A (p.Glu55Lys) rs763469464
NM_000834.5(GRIN2B):c.1655-12dup rs768388356
NM_000834.5(GRIN2B):c.1806C>T (p.Ile602=) rs1805522
NM_000834.5(GRIN2B):c.188C>T (p.Ser63Phe) rs1865821627
NM_000834.5(GRIN2B):c.189C>A (p.Ser63=) rs199707487
NM_000834.5(GRIN2B):c.2172-10del rs761900678
NM_000834.5(GRIN2B):c.2172-15dup rs761900678
NM_000834.5(GRIN2B):c.2202A>G (p.Ala734=) rs148185805
NM_000834.5(GRIN2B):c.2538C>A (p.Phe846Leu) rs1414370305
NM_000834.5(GRIN2B):c.2552T>C (p.Met851Thr)
NM_000834.5(GRIN2B):c.2665G>A (p.Ala889Thr) rs756224637
NM_000834.5(GRIN2B):c.2698C>T (p.Arg900Cys)
NM_000834.5(GRIN2B):c.2717A>G (p.Lys906Arg)
NM_000834.5(GRIN2B):c.2745T>A (p.Asn915Lys)
NM_000834.5(GRIN2B):c.274C>A (p.Arg92=) rs1436757161
NM_000834.5(GRIN2B):c.278A>G (p.Lys93Arg) rs1865819544
NM_000834.5(GRIN2B):c.2810A>G (p.His937Arg) rs1168893427
NM_000834.5(GRIN2B):c.2816G>T (p.Arg939Leu)
NM_000834.5(GRIN2B):c.2854C>T (p.Pro952Ser) rs1565454641
NM_000834.5(GRIN2B):c.2960A>G (p.His987Arg) rs765183831
NM_000834.5(GRIN2B):c.2975A>G (p.His992Arg) rs1555102461
NM_000834.5(GRIN2B):c.3028C>T (p.Pro1010Ser)
NM_000834.5(GRIN2B):c.3043T>G (p.Ser1015Ala) rs574130239
NM_000834.5(GRIN2B):c.3082C>T (p.Pro1028Ser)
NM_000834.5(GRIN2B):c.3127T>G (p.Ser1043Ala) rs1251332746
NM_000834.5(GRIN2B):c.313C>G (p.Gln105Glu)
NM_000834.5(GRIN2B):c.3141C>A (p.Asp1047Glu) rs1948598797
NM_000834.5(GRIN2B):c.3160G>A (p.Asp1054Asn)
NM_000834.5(GRIN2B):c.3233C>G (p.Ala1078Gly)
NM_000834.5(GRIN2B):c.3326A>G (p.Tyr1109Cys) rs1948594046
NM_000834.5(GRIN2B):c.3340C>T (p.Pro1114Ser) rs2136404905
NM_000834.5(GRIN2B):c.3344G>A (p.Arg1115His) rs199514711
NM_000834.5(GRIN2B):c.3365A>G (p.Tyr1122Cys) rs749285212
NM_000834.5(GRIN2B):c.3389G>T (p.Arg1130Leu) rs148625092
NM_000834.5(GRIN2B):c.3413G>T (p.Arg1138Leu) rs187979330
NM_000834.5(GRIN2B):c.3473G>T (p.Arg1158Leu) rs143955920
NM_000834.5(GRIN2B):c.3497C>G (p.Ser1166Cys)
NM_000834.5(GRIN2B):c.3543C>A (p.His1181Gln) rs866476716
NM_000834.5(GRIN2B):c.3550G>A (p.Gly1184Ser)
NM_000834.5(GRIN2B):c.362C>T (p.Thr121Ile)
NM_000834.5(GRIN2B):c.3641T>C (p.Phe1214Ser)
NM_000834.5(GRIN2B):c.3673T>A (p.Tyr1225Asn) rs1591605873
NM_000834.5(GRIN2B):c.3703G>A (p.Gly1235Ser) rs886049099
NM_000834.5(GRIN2B):c.370C>G (p.Leu124Val)
NM_000834.5(GRIN2B):c.3722G>A (p.Arg1241Gln) rs2136403871
NM_000834.5(GRIN2B):c.3792C>G (p.Asp1264Glu)
NM_000834.5(GRIN2B):c.3886A>C (p.Asn1296His) rs1555101871
NM_000834.5(GRIN2B):c.38G>T (p.Trp13Leu) rs765133670
NM_000834.5(GRIN2B):c.3943G>A (p.Ala1315Thr)
NM_000834.5(GRIN2B):c.3950T>C (p.Leu1317Pro) rs2136403363
NM_000834.5(GRIN2B):c.3964G>T (p.Val1322Leu)
NM_000834.5(GRIN2B):c.3991A>C (p.Met1331Leu) rs1338505023
NM_000834.5(GRIN2B):c.4021G>C (p.Glu1341Gln)
NM_000834.5(GRIN2B):c.4031C>T (p.Ala1344Val) rs759438353
NM_000834.5(GRIN2B):c.4075G>T (p.Ala1359Ser) rs2136403015
NM_000834.5(GRIN2B):c.4102G>T (p.Gly1368Cys)
NM_000834.5(GRIN2B):c.4114A>G (p.Met1372Val)
NM_000834.5(GRIN2B):c.4162A>G (p.Ile1388Val)
NM_000834.5(GRIN2B):c.4229C>G (p.Thr1410Arg) rs779830552
NM_000834.5(GRIN2B):c.4289T>C (p.Val1430Ala)
NM_000834.5(GRIN2B):c.4300C>T (p.Leu1434Phe) rs1002108827
NM_000834.5(GRIN2B):c.4307G>C (p.Gly1436Ala) rs1565452616
NM_000834.5(GRIN2B):c.4312G>A (p.Val1438Met) rs763699668
NM_000834.5(GRIN2B):c.4337T>A (p.Ile1446Asn)
NM_000834.5(GRIN2B):c.4359C>A (p.Asn1453Lys)
NM_000834.5(GRIN2B):c.465C>A (p.Ser155=) rs115189840
NM_000834.5(GRIN2B):c.511A>G (p.Ile171Val)
NM_000834.5(GRIN2B):c.627G>A (p.Leu209=)
NM_000834.5(GRIN2B):c.76G>A (p.Ala26Thr) rs79962661
NM_000834.5(GRIN2B):c.80G>T (p.Arg27Leu) rs200727145
NM_000834.5(GRIN2B):c.812C>A (p.Ala271Glu) rs138098032
NM_000834.5(GRIN2B):c.856G>C (p.Asp286His)
NM_000834.5(GRIN2B):c.868C>T (p.Pro290Ser) rs1863522709
NM_000834.5(GRIN2B):c.92G>C (p.Ser31Thr) rs746004289
NM_000834.5(GRIN2B):c.94C>A (p.Pro32Thr)
NM_000834.5(GRIN2B):c.959G>C (p.Ser320Thr) rs931791422
NM_000834.5(GRIN2B):c.992A>G (p.Gln331Arg) rs1555132930

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