ClinVar Miner

List of variants in gene GRIN2B reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 110
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
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.2861G>A (p.Cys954Tyr) rs376328340 0.00003
NM_000834.5(GRIN2B):c.3499G>A (p.Val1167Ile) rs1042339 0.00002
NM_000834.5(GRIN2B):c.3964G>A (p.Val1322Ile) rs200255226 0.00002
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.1559C>T (p.Ser520Leu) rs1211941493 0.00001
NM_000834.5(GRIN2B):c.2497C>G (p.Leu833Val) rs1439435536 0.00001
NM_000834.5(GRIN2B):c.2530T>C (p.Trp844Arg) rs138088984 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.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.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.3878A>G (p.Lys1293Arg) rs749655702 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.4265G>A (p.Arg1422Gln) rs75269586 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
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.1329G>C (p.Glu443Asp)
NM_000834.5(GRIN2B):c.1745C>G (p.Pro582Arg) rs796052581
NM_000834.5(GRIN2B):c.1946A>C (p.Asn649Thr) rs879253945
NM_000834.5(GRIN2B):c.1976A>T (p.Tyr659Phe) rs2136470266
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.2308T>G (p.Ser770Ala) rs2136413207
NM_000834.5(GRIN2B):c.2372A>T (p.Glu791Val)
NM_000834.5(GRIN2B):c.2393C>G (p.Thr798Ser) rs1948652982
NM_000834.5(GRIN2B):c.2498T>C (p.Leu833Pro)
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.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.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.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.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.3343C>T (p.Arg1115Cys)
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.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.377T>C (p.Ile126Thr) rs879254008
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.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.4062_4127del (p.Ser1355_Ser1376del) rs2136402892
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.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.4300C>T (p.Leu1434Phe) rs1002108827
NM_000834.5(GRIN2B):c.4312G>A (p.Val1438Met) rs763699668
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.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.811G>A (p.Ala271Thr) rs1863525014
NM_000834.5(GRIN2B):c.841T>A (p.Ser281Thr) rs1085307651
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.969C>A (p.Asn323Lys)
NM_000834.5(GRIN2B):c.976G>A (p.Glu326Lys) rs1555132947
NM_000834.5(GRIN2B):c.983G>T (p.Arg328Ile)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.