ClinVar Miner

List of variants in gene GRIN2A reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 107
Download table as spreadsheet
HGVS dbSNP
NM_000833.5(GRIN2A):c.-190C>G rs771301601
NM_000833.5(GRIN2A):c.-190C>T rs771301601
NM_000833.5(GRIN2A):c.-209-6C>T rs1057521259
NM_000833.5(GRIN2A):c.-215G>C rs1057518450
NM_000833.5(GRIN2A):c.-215G>T rs1057518450
NM_000833.5(GRIN2A):c.-34C>G rs564039694
NM_000833.5(GRIN2A):c.1007+13T>G rs199862009
NM_000833.5(GRIN2A):c.1007+6A>G rs1427858640
NM_000833.5(GRIN2A):c.1008-14C>T rs776960433
NM_000833.5(GRIN2A):c.1069G>A (p.Val357Met) rs78929970
NM_000833.5(GRIN2A):c.1141C>T (p.His381Tyr) rs757464009
NM_000833.5(GRIN2A):c.1305A>T (p.Pro435=) rs1555496114
NM_000833.5(GRIN2A):c.1437G>A (p.Leu479=) rs768988228
NM_000833.5(GRIN2A):c.1494T>C (p.Gly498=) rs777998695
NM_000833.5(GRIN2A):c.1498-11C>T rs759632014
NM_000833.5(GRIN2A):c.1509A>G (p.Gln503=) rs1261235589
NM_000833.5(GRIN2A):c.1533G>A (p.Ser511=) rs112848130
NM_000833.5(GRIN2A):c.1652-19T>C rs778659119
NM_000833.5(GRIN2A):c.1652-6T>C rs1057521713
NM_000833.5(GRIN2A):c.1667C>T (p.Ser556Phe) rs587780349
NM_000833.5(GRIN2A):c.1728T>C (p.Phe576=) rs540499505
NM_000833.5(GRIN2A):c.1842T>C (p.Asn614=) rs138236719
NM_000833.5(GRIN2A):c.2007+11C>G rs758596798
NM_000833.5(GRIN2A):c.2049G>C (p.Gly683=) rs1057523027
NM_000833.5(GRIN2A):c.2070G>A (p.Thr690=) rs141924924
NM_000833.5(GRIN2A):c.2202C>G (p.Val734=) rs367543138
NM_000833.5(GRIN2A):c.2356+6A>T rs1030132899
NM_000833.5(GRIN2A):c.2406C>T (p.Asn802=) rs748977420
NM_000833.5(GRIN2A):c.252G>T (p.Thr84=) rs140136379
NM_000833.5(GRIN2A):c.2566C>A (p.Arg856=) rs201072838
NM_000833.5(GRIN2A):c.2595+12G>A rs746566593
NM_000833.5(GRIN2A):c.2595+16G>A rs779583842
NM_000833.5(GRIN2A):c.2640G>A (p.Lys880=) rs778938265
NM_000833.5(GRIN2A):c.2930A>G (p.Asn977Ser) rs1555482808
NM_000833.5(GRIN2A):c.294C>T (p.Leu98=) rs771068226
NM_000833.5(GRIN2A):c.2958T>G (p.Leu986=) rs1057522359
NM_000833.5(GRIN2A):c.2985G>A (p.Thr995=) rs781646325
NM_000833.5(GRIN2A):c.3030C>T (p.Pro1010=) rs763891276
NM_000833.5(GRIN2A):c.3246C>G (p.Thr1082=) rs143039009
NM_000833.5(GRIN2A):c.3246C>T (p.Thr1082=) rs143039009
NM_000833.5(GRIN2A):c.3387C>T (p.His1129=) rs1223085313
NM_000833.5(GRIN2A):c.3492G>A (p.Thr1164=) rs1330743809
NM_000833.5(GRIN2A):c.3553A>G (p.Lys1185Glu) rs587780354
NM_000833.5(GRIN2A):c.3624G>A (p.Arg1208=) rs587780350
NM_000833.5(GRIN2A):c.3627G>A (p.Gln1209=) rs1191216428
NM_000833.5(GRIN2A):c.3882C>T (p.Asn1294=) rs1057522011
NM_000833.5(GRIN2A):c.3898A>G (p.Arg1300Gly) rs372353067
NM_000833.5(GRIN2A):c.3909C>T (p.Asp1303=) rs765744766
NM_000833.5(GRIN2A):c.4011G>A (p.Ser1337=) rs748586367
NM_000833.5(GRIN2A):c.415-11T>G rs1320602728
NM_000833.5(GRIN2A):c.415-15T>C rs1057522859
NM_000833.5(GRIN2A):c.4170G>A (p.Ser1390=) rs1057522803
NM_000833.5(GRIN2A):c.420G>A (p.Pro140=) rs367543126
NM_000833.5(GRIN2A):c.468G>T (p.Thr156=) rs773513210
NM_000833.5(GRIN2A):c.561C>T (p.Val187=) rs1057521908
NM_000833.5(GRIN2A):c.687C>T (p.Leu229=) rs372649219
NM_000833.5(GRIN2A):c.744C>T (p.Leu248=) rs928714067
NM_000833.5(GRIN2A):c.747C>T (p.Thr249=) rs774169125
NM_000833.5(GRIN2A):c.801C>T (p.Leu267=) rs1186955038
NM_000833.5(GRIN2A):c.822G>A (p.Ser274=) rs759344136
NM_000833.5(GRIN2A):c.990G>A (p.Pro330=) rs149902963
NM_000833.5(GRIN2A):c.990G>T (p.Pro330=) rs149902963
NM_001134407.3(GRIN2A):c.1275G>A (p.Leu425=) rs2229193
NM_001134407.3(GRIN2A):c.1284G>A (p.Thr428=) rs147211564
NM_001134407.3(GRIN2A):c.1329-8C>T rs7193290
NM_001134407.3(GRIN2A):c.1329-9T>G rs541442732
NM_001134407.3(GRIN2A):c.1354G>A (p.Val452Met) rs145956175
NM_001134407.3(GRIN2A):c.1428C>T (p.Asp476=) rs762674544
NM_001134407.3(GRIN2A):c.1458C>A (p.Gly486=) rs144572467
NM_001134407.3(GRIN2A):c.1593G>A (p.Thr531=) rs957436270
NM_001134407.3(GRIN2A):c.1629C>T (p.Thr543=) rs758378272
NM_001134407.3(GRIN2A):c.2007+10C>T rs368110989
NM_001134407.3(GRIN2A):c.2085G>C (p.Arg695=) rs9806806
NM_001134407.3(GRIN2A):c.2250C>T (p.Ile750=) rs143779792
NM_001134407.3(GRIN2A):c.2277C>T (p.Thr759=) rs148846694
NM_001134407.3(GRIN2A):c.2478C>T (p.Ala826=) rs373628160
NM_001134407.3(GRIN2A):c.2505C>T (p.Phe835=) rs771342023
NM_001134407.3(GRIN2A):c.2627T>C (p.Ile876Thr) rs199784503
NM_001134407.3(GRIN2A):c.2664G>A (p.Thr888=) rs113847665
NM_001134407.3(GRIN2A):c.2735C>G (p.Ser912Cys) rs200588845
NM_001134407.3(GRIN2A):c.2852G>T (p.Gly951Val) rs139795367
NM_001134407.3(GRIN2A):c.2883C>T (p.Asn961=) rs77705198
NM_001134407.3(GRIN2A):c.288C>T (p.His96=) rs74853460
NM_001134407.3(GRIN2A):c.2899G>C (p.Val967Leu) rs61731465
NM_001134407.3(GRIN2A):c.3003C>T (p.Ser1001=) rs199551487
NM_001134407.3(GRIN2A):c.306C>T (p.Asp102=) rs200850130
NM_001134407.3(GRIN2A):c.3103G>A (p.Asp1035Asn) rs540445580
NM_001134407.3(GRIN2A):c.3190A>G (p.Thr1064Ala) rs138809301
NM_001134407.3(GRIN2A):c.3276C>G (p.Ser1092=) rs775325646
NM_001134407.3(GRIN2A):c.3363T>G (p.Asp1121Glu) rs764292783
NM_001134407.3(GRIN2A):c.3400C>A (p.Gln1134Lys) rs748967552
NM_001134407.3(GRIN2A):c.3426C>T (p.Pro1142=) rs150487431
NM_001134407.3(GRIN2A):c.3468A>T (p.Glu1156Asp) rs778180100
NM_001134407.3(GRIN2A):c.3827C>G (p.Ala1276Gly) rs145063086
NM_001134407.3(GRIN2A):c.402C>T (p.Ile134=) rs587780352
NM_001134407.3(GRIN2A):c.4185G>A (p.Ala1395=) rs778429009
NM_001134407.3(GRIN2A):c.422C>T (p.Thr141Met) rs78631453
NM_001134407.3(GRIN2A):c.4307A>G (p.Asn1436Ser) rs77029288
NM_001134407.3(GRIN2A):c.4356C>G (p.Arg1452=) rs140093291
NM_001134407.3(GRIN2A):c.547T>A (p.Phe183Ile) rs587780353
NM_001134407.3(GRIN2A):c.662A>G (p.Lys221Arg) rs61731464
NM_001134407.3(GRIN2A):c.666C>T (p.Ile222=) rs143594020
NM_001134407.3(GRIN2A):c.741C>T (p.Gly247=) rs141912603
NM_001134407.3(GRIN2A):c.76G>T (p.Ala26Ser) rs751198815
NM_001134407.3(GRIN2A):c.903C>T (p.Thr301=) rs78241448
NM_001134407.3(GRIN2A):c.949A>C (p.Lys317Gln) rs141326581
NM_001134407.3(GRIN2A):c.963C>T (p.Tyr321=) rs368200727

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.