ClinVar Miner

List of variants in gene GRIN2B reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 167
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HGVS dbSNP gnomAD frequency
NM_000834.5(GRIN2B):c.2931C>G (p.Asp977Glu) rs147956755 0.00029
NM_000834.5(GRIN2B):c.3076G>A (p.Gly1026Ser) rs201963596 0.00011
NM_000834.5(GRIN2B):c.1768G>A (p.Ala590Thr) rs145021339 0.00006
NM_000834.5(GRIN2B):c.3047G>A (p.Arg1016Lys) rs141109968 0.00006
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.251G>A (p.Arg84His) rs778695605 0.00003
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.-10C>T rs200539507 0.00001
NM_000834.5(GRIN2B):c.125T>C (p.Val42Ala) rs796052580 0.00001
NM_000834.5(GRIN2B):c.136G>A (p.Asp46Asn) rs370809599 0.00001
NM_000834.5(GRIN2B):c.1559C>T (p.Ser520Leu) rs1211941493 0.00001
NM_000834.5(GRIN2B):c.2497C>G (p.Leu833Val) rs1439435536 0.00001
NM_000834.5(GRIN2B):c.2627C>T (p.Ala876Val) rs1458368988 0.00001
NM_000834.5(GRIN2B):c.2759G>A (p.Ser920Asn) rs781442804 0.00001
NM_000834.5(GRIN2B):c.2855C>T (p.Pro952Leu) rs747714077 0.00001
NM_000834.5(GRIN2B):c.286G>C (p.Gly96Arg) rs1865819395 0.00001
NM_000834.5(GRIN2B):c.2936A>T (p.Asn979Ile) rs796052574 0.00001
NM_000834.5(GRIN2B):c.3056G>T (p.Ser1019Ile) rs200265732 0.00001
NM_000834.5(GRIN2B):c.3099C>G (p.Ser1033Arg) rs796052575 0.00001
NM_000834.5(GRIN2B):c.3118G>A (p.Gly1040Ser) rs202222002 0.00001
NM_000834.5(GRIN2B):c.3137G>T (p.Ser1046Ile) rs201029083 0.00001
NM_000834.5(GRIN2B):c.3170G>A (p.Arg1057His) rs773737239 0.00001
NM_000834.5(GRIN2B):c.3202G>A (p.Val1068Ile) rs749434579 0.00001
NM_000834.5(GRIN2B):c.3344G>T (p.Arg1115Leu) rs199514711 0.00001
NM_000834.5(GRIN2B):c.3365A>C (p.Tyr1122Ser) rs749285212 0.00001
NM_000834.5(GRIN2B):c.3383G>C (p.Gly1128Ala) rs769658975 0.00001
NM_000834.5(GRIN2B):c.3626G>A (p.Arg1209Gln) rs748005909 0.00001
NM_000834.5(GRIN2B):c.36C>A (p.Phe12Leu) rs752668123 0.00001
NM_000834.5(GRIN2B):c.381C>T (p.His127=) rs200608452 0.00001
NM_000834.5(GRIN2B):c.3878A>G (p.Lys1293Arg) rs749655702 0.00001
NM_000834.5(GRIN2B):c.4049C>T (p.Ala1350Val) rs763372245 0.00001
NM_000834.5(GRIN2B):c.4112A>G (p.Tyr1371Cys) rs755797497 0.00001
NM_000834.5(GRIN2B):c.4142G>A (p.Arg1381Gln) rs761443441 0.00001
NM_000834.5(GRIN2B):c.4205A>G (p.Lys1402Arg) rs1349506481 0.00001
NM_000834.5(GRIN2B):c.4244C>T (p.Ser1415Leu) rs201463390 0.00001
NM_000834.5(GRIN2B):c.4265G>A (p.Arg1422Gln) rs75269586 0.00001
NM_000834.5(GRIN2B):c.4341T>C (p.Cys1447=) rs766970197 0.00001
NM_000834.5(GRIN2B):c.4355C>T (p.Ser1452Phe) rs756790727 0.00001
NM_000834.5(GRIN2B):c.4400G>C (p.Gly1467Ala) rs200127692 0.00001
NM_000834.5(GRIN2B):c.679A>G (p.Ile227Val) rs201672517 0.00001
NM_000834.5(GRIN2B):c.935G>A (p.Ser312Asn) rs1085307687 0.00001
GRCh37/hg19 12p13.1(chr12:13722312-13788885)x3
GRCh37/hg19 12p13.1(chr12:13772992-13796378)x1
NM_000834.5(GRIN2B):c.104T>C (p.Ile35Thr) rs201568626
NM_000834.5(GRIN2B):c.1126-3C>T rs1555112424
NM_000834.5(GRIN2B):c.1175C>T (p.Pro392Leu)
NM_000834.5(GRIN2B):c.1277G>A (p.Ser426Asn) rs2136481263
NM_000834.5(GRIN2B):c.1288A>C (p.Met430Leu)
NM_000834.5(GRIN2B):c.1329G>C (p.Glu443Asp)
NM_000834.5(GRIN2B):c.1393C>G (p.Leu465Val) rs2136480027
NM_000834.5(GRIN2B):c.1427A>G (p.Tyr476Cys)
NM_000834.5(GRIN2B):c.1429G>T (p.Asp477Tyr) rs2136479969
NM_000834.5(GRIN2B):c.1705G>A (p.Val569Ile) rs1293991066
NM_000834.5(GRIN2B):c.1745C>G (p.Pro582Arg) rs796052581
NM_000834.5(GRIN2B):c.1767C>G (p.Leu589=) rs763286576
NM_000834.5(GRIN2B):c.1783C>T (p.Pro595Ser) rs766030730
NM_000834.5(GRIN2B):c.1807G>C (p.Gly603Arg) rs1156304737
NM_000834.5(GRIN2B):c.1976A>T (p.Tyr659Phe) rs2136470266
NM_000834.5(GRIN2B):c.2001C>A (p.Ser667Arg) rs200392452
NM_000834.5(GRIN2B):c.200G>A (p.Arg67Gln)
NM_000834.5(GRIN2B):c.2011-4C>T rs1447482208
NM_000834.5(GRIN2B):c.2138G>T (p.Gly713Val) rs1454642871
NM_000834.5(GRIN2B):c.2179G>T (p.Asp727Tyr) rs2136413432
NM_000834.5(GRIN2B):c.2192A>T (p.Tyr731Phe) rs1948686521
NM_000834.5(GRIN2B):c.2200G>A (p.Ala734Thr) rs886044569
NM_000834.5(GRIN2B):c.2260G>A (p.Gly754Arg) rs1555103635
NM_000834.5(GRIN2B):c.2308T>G (p.Ser770Ala) rs2136413207
NM_000834.5(GRIN2B):c.2311G>C (p.Gly771Arg)
NM_000834.5(GRIN2B):c.2372A>T (p.Glu791Val)
NM_000834.5(GRIN2B):c.2393C>G (p.Thr798Ser) rs1948652982
NM_000834.5(GRIN2B):c.2487G>A (p.Met829Ile)
NM_000834.5(GRIN2B):c.2498T>C (p.Leu833Pro)
NM_000834.5(GRIN2B):c.2543A>G (p.His848Arg) rs1064797166
NM_000834.5(GRIN2B):c.2557_2558del (p.Val853fs) rs876661022
NM_000834.5(GRIN2B):c.2572C>T (p.Pro858Ser) rs2136409452
NM_000834.5(GRIN2B):c.2613C>T (p.Cys871=) rs1555102646
NM_000834.5(GRIN2B):c.2638C>G (p.Arg880Gly)
NM_000834.5(GRIN2B):c.2639G>A (p.Arg880His) rs904771425
NM_000834.5(GRIN2B):c.2662A>G (p.Thr888Ala) rs200256539
NM_000834.5(GRIN2B):c.2676C>A (p.Asn892Lys) rs2136406314
NM_000834.5(GRIN2B):c.2692A>T (p.Ile898Phe) rs2136406285
NM_000834.5(GRIN2B):c.2773A>G (p.Ile925Val)
NM_000834.5(GRIN2B):c.28C>A (p.Pro10Thr) rs1164700607
NM_000834.5(GRIN2B):c.2964C>A (p.His988Gln) rs1197717686
NM_000834.5(GRIN2B):c.2972C>T (p.Pro991Leu)
NM_000834.5(GRIN2B):c.2986_2994del (p.Ala997_Ser999del)
NM_000834.5(GRIN2B):c.29C>A (p.Pro10His) rs898703967
NM_000834.5(GRIN2B):c.3040C>A (p.Gln1014Lys) rs1555102419
NM_000834.5(GRIN2B):c.3043T>G (p.Ser1015Ala) rs574130239
NM_000834.5(GRIN2B):c.3135_3149del (p.Lys1045_Ser1050delinsAsn) rs2136405352
NM_000834.5(GRIN2B):c.3146A>G (p.Tyr1049Cys) rs201866998
NM_000834.5(GRIN2B):c.3200C>T (p.Thr1067Ile) rs1555102353
NM_000834.5(GRIN2B):c.3208T>C (p.Tyr1070His) rs2136405228
NM_000834.5(GRIN2B):c.3219C>G (p.Ile1073Met)
NM_000834.5(GRIN2B):c.3241C>A (p.Arg1081Ser) rs796052576
NM_000834.5(GRIN2B):c.324C>T (p.Ile108=)
NM_000834.5(GRIN2B):c.3257_3277del (p.Lys1086_Pro1093delinsThr) rs2136405055
NM_000834.5(GRIN2B):c.325G>T (p.Ala109Ser) rs772078838
NM_000834.5(GRIN2B):c.3290A>C (p.Lys1097Thr)
NM_000834.5(GRIN2B):c.3301G>T (p.Glu1101Ter) rs1555102308
NM_000834.5(GRIN2B):c.3326A>G (p.Tyr1109Cys) rs1948594046
NM_000834.5(GRIN2B):c.3329G>A (p.Arg1110His) rs1271239566
NM_000834.5(GRIN2B):c.3343C>T (p.Arg1115Cys)
NM_000834.5(GRIN2B):c.3372G>A (p.Arg1124=)
NM_000834.5(GRIN2B):c.337G>A (p.Asp113Asn) rs2136746973
NM_000834.5(GRIN2B):c.3408G>C (p.Gln1136His)
NM_000834.5(GRIN2B):c.3413G>T (p.Arg1138Leu) rs187979330
NM_000834.5(GRIN2B):c.3446T>C (p.Val1149Ala)
NM_000834.5(GRIN2B):c.3496T>A (p.Ser1166Thr)
NM_000834.5(GRIN2B):c.3625C>G (p.Arg1209Gly)
NM_000834.5(GRIN2B):c.3635G>A (p.Gly1212Asp) rs1233916467
NM_000834.5(GRIN2B):c.3646C>T (p.Arg1216Cys) rs199834850
NM_000834.5(GRIN2B):c.364C>T (p.Pro122Ser) rs1865817808
NM_000834.5(GRIN2B):c.365_366delinsTG (p.Pro122Leu) rs2136746928
NM_000834.5(GRIN2B):c.3670_3672del (p.Asn1224del) rs1555102005
NM_000834.5(GRIN2B):c.3745G>T (p.Gly1249Cys) rs796052577
NM_000834.5(GRIN2B):c.3834C>A (p.Thr1278=)
NM_000834.5(GRIN2B):c.3883C>T (p.Arg1295Trp) rs560662030
NM_000834.5(GRIN2B):c.3890A>G (p.Lys1297Arg) rs916745822
NM_000834.5(GRIN2B):c.3893T>C (p.Leu1298Pro) rs876661100
NM_000834.5(GRIN2B):c.38G>T (p.Trp13Leu) rs765133670
NM_000834.5(GRIN2B):c.392C>T (p.Ser131Phe)
NM_000834.5(GRIN2B):c.3942A>T (p.Glu1314Asp) rs2136403386
NM_000834.5(GRIN2B):c.3955C>T (p.Pro1319Ser)
NM_000834.5(GRIN2B):c.3958C>T (p.Arg1320Cys) rs2136403344
NM_000834.5(GRIN2B):c.3994G>T (p.Asp1332Tyr)
NM_000834.5(GRIN2B):c.3995_3997dup (p.Asp1332_Gly1333insAsp)
NM_000834.5(GRIN2B):c.4040G>A (p.Ser1347Asn) rs772733555
NM_000834.5(GRIN2B):c.4050CAA[2] (p.Asn1352del) rs761812510
NM_000834.5(GRIN2B):c.4062_4127del (p.Ser1355_Ser1376del) rs2136402892
NM_000834.5(GRIN2B):c.4084CAC[2] (p.His1364del) rs1214837315
NM_000834.5(GRIN2B):c.411+4A>C
NM_000834.5(GRIN2B):c.4120A>C (p.Ser1374Arg) rs2136402897
NM_000834.5(GRIN2B):c.4183C>A (p.Gln1395Lys) rs1555101663
NM_000834.5(GRIN2B):c.4206A>C (p.Lys1402Asn)
NM_000834.5(GRIN2B):c.4208C>T (p.Ser1403Phe) rs1948569956
NM_000834.5(GRIN2B):c.4232T>G (p.Val1411Gly) rs1555101622
NM_000834.5(GRIN2B):c.4244C>G (p.Ser1415Trp)
NM_000834.5(GRIN2B):c.4261T>C (p.Phe1421Leu) rs879254129
NM_000834.5(GRIN2B):c.4288G>C (p.Val1430Leu) rs879253885
NM_000834.5(GRIN2B):c.4292T>C (p.Val1431Ala) rs1555101581
NM_000834.5(GRIN2B):c.4299C>T (p.Ala1433=)
NM_000834.5(GRIN2B):c.4300C>T (p.Leu1434Phe) rs1002108827
NM_000834.5(GRIN2B):c.4312G>A (p.Val1438Met) rs763699668
NM_000834.5(GRIN2B):c.4374CAA[1] (p.Asn1459del)
NM_000834.5(GRIN2B):c.4409A>G (p.Asn1470Ser)
NM_000834.5(GRIN2B):c.466G>A (p.Val156Ile) rs1555133189
NM_000834.5(GRIN2B):c.471G>C (p.Met157Ile) rs876661185
NM_000834.5(GRIN2B):c.512T>A (p.Ile171Asn)
NM_000834.5(GRIN2B):c.544T>G (p.Phe182Val)
NM_000834.5(GRIN2B):c.623C>T (p.Ser208Phe)
NM_000834.5(GRIN2B):c.63_64delinsTG (p.Ser22Ala) rs2136747439
NM_000834.5(GRIN2B):c.730G>T (p.Ala244Ser) rs1555133062
NM_000834.5(GRIN2B):c.764C>T (p.Thr255Met) rs748054907
NM_000834.5(GRIN2B):c.805G>C (p.Val269Leu)
NM_000834.5(GRIN2B):c.811G>A (p.Ala271Thr) rs1863525014
NM_000834.5(GRIN2B):c.841T>A (p.Ser281Thr) rs1085307651
NM_000834.5(GRIN2B):c.857A>G (p.Asp286Gly)
NM_000834.5(GRIN2B):c.876A>G (p.Arg292=) rs876661173
NM_000834.5(GRIN2B):c.914C>T (p.Ser305Phe) rs2136628926
NM_000834.5(GRIN2B):c.94C>A (p.Pro32Thr)
NM_000834.5(GRIN2B):c.969C>A (p.Asn323Lys)
NM_000834.5(GRIN2B):c.976G>A (p.Glu326Lys) rs1555132947
NM_000834.5(GRIN2B):c.983G>T (p.Arg328Ile)

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