ClinVar Miner

List of variants in gene GRIN2A studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 143
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001134407.3(GRIN2A):c.2085G>C (p.Arg695=) rs9806806 0.33435
NM_001134407.3(GRIN2A):c.1275G>A (p.Leu425=) rs2229193 0.27838
NM_001134407.3(GRIN2A):c.1008-16C>G rs9932916 0.03409
NM_001134407.3(GRIN2A):c.1329-8C>T rs7193290 0.01998
NM_001134407.3(GRIN2A):c.2190C>T (p.Tyr730=) rs61753382 0.00763
NM_001134407.3(GRIN2A):c.2899G>C (p.Val967Leu) rs61731465 0.00502
NM_001134407.3(GRIN2A):c.3228C>A (p.Asn1076Lys) rs61758995 0.00472
NM_001134407.3(GRIN2A):c.662A>G (p.Lys221Arg) rs61731464 0.00322
NM_001134407.3(GRIN2A):c.1652-13T>C rs201444481 0.00226
NM_001134407.3(GRIN2A):c.1251C>T (p.Val417=) rs139329447 0.00150
NM_001134407.3(GRIN2A):c.3622C>A (p.Arg1208=) rs78544202 0.00143
NM_001134407.3(GRIN2A):c.-34C>A rs564039694 0.00134
NM_001134407.3(GRIN2A):c.1777+17G>A rs375869375 0.00134
NM_001134407.3(GRIN2A):c.900C>T (p.Thr300=) rs143669998 0.00133
NM_001134407.3(GRIN2A):c.903C>T (p.Thr301=) rs78241448 0.00119
NM_001134407.3(GRIN2A):c.2007+15C>T rs76627672 0.00114
NM_001134407.3(GRIN2A):c.1354G>A (p.Val452Met) rs145956175 0.00105
NM_001134407.3(GRIN2A):c.-19+8C>T rs563518225 0.00084
NM_001134407.3(GRIN2A):c.669C>T (p.His223=) rs138117658 0.00076
NM_001134407.3(GRIN2A):c.4307A>G (p.Asn1436Ser) rs77029288 0.00068
NM_001134407.3(GRIN2A):c.3827C>G (p.Ala1276Gly) rs145063086 0.00067
NM_001134407.3(GRIN2A):c.2883C>T (p.Asn961=) rs77705198 0.00059
NM_001134407.3(GRIN2A):c.3190A>G (p.Thr1064Ala) rs138809301 0.00055
NM_001134407.3(GRIN2A):c.2852G>T (p.Gly951Val) rs139795367 0.00042
NM_001134407.3(GRIN2A):c.-220C>T rs139646156 0.00037
NM_001134407.3(GRIN2A):c.939C>T (p.Ile313=) rs146867324 0.00030
NM_001134407.3(GRIN2A):c.1410T>G (p.Thr470=) rs372058698 0.00028
NM_001134407.3(GRIN2A):c.2007+16T>C rs371738664 0.00026
NM_001134407.3(GRIN2A):c.2277C>T (p.Thr759=) rs148846694 0.00024
NM_001134407.3(GRIN2A):c.736C>A (p.Leu246Ile) rs555768104 0.00021
NM_001134407.3(GRIN2A):c.1458C>A (p.Gly486=) rs144572467 0.00019
NM_001134407.3(GRIN2A):c.2007+10C>T rs368110989 0.00019
NM_001134407.3(GRIN2A):c.819A>G (p.Pro273=) rs148085725 0.00013
NM_001134407.3(GRIN2A):c.2008-14C>T rs375126711 0.00012
NM_001134407.3(GRIN2A):c.949A>C (p.Lys317Gln) rs141326581 0.00011
NM_001134407.3(GRIN2A):c.1007+13T>G rs199862009 0.00009
NM_001134407.3(GRIN2A):c.1652-14C>G rs375922984 0.00009
NM_001134407.3(GRIN2A):c.447G>A (p.Ala149=) rs144464666 0.00009
NM_001134407.3(GRIN2A):c.1652-19T>C rs778659119 0.00007
NM_001134407.3(GRIN2A):c.2636A>G (p.Lys879Arg) rs183029507 0.00007
NM_001134407.3(GRIN2A):c.3898A>G (p.Arg1300Gly) rs372353067 0.00007
NM_001134407.3(GRIN2A):c.882C>T (p.Asp294=) rs201002710 0.00007
NM_001134407.3(GRIN2A):c.1141C>T (p.His381Tyr) rs757464009 0.00006
NM_001134407.3(GRIN2A):c.2250C>T (p.Ile750=) rs143779792 0.00006
NM_001134407.3(GRIN2A):c.2760A>G (p.Arg920=) rs80138441 0.00006
NM_001134407.3(GRIN2A):c.3103G>A (p.Asp1035Asn) rs540445580 0.00006
NM_001134407.3(GRIN2A):c.4170G>A (p.Ser1390=) rs1057522803 0.00006
NM_001134407.3(GRIN2A):c.623C>T (p.Thr208Ile) rs367543124 0.00006
NM_001134407.3(GRIN2A):c.1509A>G (p.Gln503=) rs1261235589 0.00005
NM_001134407.3(GRIN2A):c.252G>T (p.Thr84=) rs140136379 0.00004
NM_001134407.3(GRIN2A):c.2664G>A (p.Thr888=) rs113847665 0.00004
NM_001134407.3(GRIN2A):c.547T>A (p.Phe183Ile) rs587780353 0.00004
NM_001134407.3(GRIN2A):c.744C>T (p.Leu248=) rs928714067 0.00004
NM_001134407.3(GRIN2A):c.883G>A (p.Gly295Ser) rs568484876 0.00004
NM_001134407.3(GRIN2A):c.989C>T (p.Pro330Leu) rs367543120 0.00004
NM_001134407.3(GRIN2A):c.2478C>T (p.Ala826=) rs373628160 0.00003
NM_001134407.3(GRIN2A):c.3578T>G (p.Leu1193Trp) rs75761674 0.00003
NM_001134407.3(GRIN2A):c.3624G>A (p.Arg1208=) rs587780350 0.00003
NM_001134407.3(GRIN2A):c.1842T>C (p.Asn614=) rs138236719 0.00002
NM_001134407.3(GRIN2A):c.2543G>A (p.Cys848Tyr) rs779911797 0.00002
NM_001134407.3(GRIN2A):c.2695C>T (p.Arg899Trp) rs796052553 0.00002
NM_001134407.3(GRIN2A):c.2908C>T (p.Arg970Trp) rs765257420 0.00002
NM_001134407.3(GRIN2A):c.3037C>T (p.Leu1013=) rs775262289 0.00002
NM_001134407.3(GRIN2A):c.1007+6A>G rs1427858640 0.00001
NM_001134407.3(GRIN2A):c.1069G>A (p.Val357Met) rs78929970 0.00001
NM_001134407.3(GRIN2A):c.1284G>A (p.Thr428=) rs147211564 0.00001
NM_001134407.3(GRIN2A):c.1437G>A (p.Leu479=) rs768988228 0.00001
NM_001134407.3(GRIN2A):c.1494T>C (p.Gly498=) rs777998695 0.00001
NM_001134407.3(GRIN2A):c.1517T>C (p.Val506Ala) rs796052543 0.00001
NM_001134407.3(GRIN2A):c.1593G>A (p.Thr531=) rs957436270 0.00001
NM_001134407.3(GRIN2A):c.1675G>A (p.Val559Met) rs1476673300 0.00001
NM_001134407.3(GRIN2A):c.171C>T (p.Pro57=) rs781693549 0.00001
NM_001134407.3(GRIN2A):c.2247C>T (p.Thr749=) rs202026070 0.00001
NM_001134407.3(GRIN2A):c.2505C>T (p.Phe835=) rs771342023 0.00001
NM_001134407.3(GRIN2A):c.2595+16G>A rs779583842 0.00001
NM_001134407.3(GRIN2A):c.2640G>A (p.Lys880=) rs778938265 0.00001
NM_001134407.3(GRIN2A):c.2985G>A (p.Thr995=) rs781646325 0.00001
NM_001134407.3(GRIN2A):c.3163G>C (p.Glu1055Gln) rs370107080 0.00001
NM_001134407.3(GRIN2A):c.3636G>A (p.Thr1212=) rs765614514 0.00001
NM_001134407.3(GRIN2A):c.3722G>A (p.Arg1241Gln) rs886042648 0.00001
NM_001134407.3(GRIN2A):c.3809A>T (p.Asp1270Val) rs750649530 0.00001
NM_001134407.3(GRIN2A):c.402C>T (p.Ile134=) rs587780352 0.00001
NM_001134407.3(GRIN2A):c.415-11T>G rs1320602728 0.00001
NM_001134407.3(GRIN2A):c.495T>C (p.Tyr165=) rs569491666 0.00001
NM_001134407.3(GRIN2A):c.561C>T (p.Val187=) rs1057521908 0.00001
NM_001134407.3(GRIN2A):c.687C>T (p.Leu229=) rs372649219 0.00001
NM_001134407.3(GRIN2A):c.801C>T (p.Leu267=) rs1186955038 0.00001
NM_001134407.3(GRIN2A):c.990G>A (p.Pro330=) rs149902963 0.00001
GRCh37/hg19 16p13.2(chr16:9937979-10149238)
NM_000833.5(GRIN2A):c.-215G>C rs1057518450
NM_000833.5(GRIN2A):c.-215G>T rs1057518450
NM_001134407.3(GRIN2A):c.-190C>G rs771301601
NM_001134407.3(GRIN2A):c.-190C>T rs771301601
NM_001134407.3(GRIN2A):c.-215C>T rs1057521259
NM_001134407.3(GRIN2A):c.-34C>G rs564039694
NM_001134407.3(GRIN2A):c.1008-14C>T rs776960433
NM_001134407.3(GRIN2A):c.1305A>T (p.Pro435=) rs1555496114
NM_001134407.3(GRIN2A):c.1329-7dup rs1455515948
NM_001134407.3(GRIN2A):c.1374G>A (p.Gly458=) rs368221866
NM_001134407.3(GRIN2A):c.1428C>T (p.Asp476=) rs762674544
NM_001134407.3(GRIN2A):c.1498-11C>T rs759632014
NM_001134407.3(GRIN2A):c.1498-14del rs745951746
NM_001134407.3(GRIN2A):c.1652-6T>C rs1057521713
NM_001134407.3(GRIN2A):c.1667C>T (p.Ser556Phe) rs587780349
NM_001134407.3(GRIN2A):c.1728T>C (p.Phe576=) rs540499505
NM_001134407.3(GRIN2A):c.1777+6G>T rs76549675
NM_001134407.3(GRIN2A):c.1A>T (p.Met1Leu)
NM_001134407.3(GRIN2A):c.2007+11C>G rs758596798
NM_001134407.3(GRIN2A):c.2049G>C (p.Gly683=) rs1057523027
NM_001134407.3(GRIN2A):c.225C>T (p.Asn75=) rs527686036
NM_001134407.3(GRIN2A):c.2325C>T (p.Ile775=) rs748291723
NM_001134407.3(GRIN2A):c.2356+6A>T rs1030132899
NM_001134407.3(GRIN2A):c.2406C>T (p.Asn802=) rs748977420
NM_001134407.3(GRIN2A):c.2595+12G>A rs746566593
NM_001134407.3(GRIN2A):c.2627T>C (p.Ile876Thr) rs199784503
NM_001134407.3(GRIN2A):c.2694C>T (p.Leu898=) rs569998469
NM_001134407.3(GRIN2A):c.2930A>G (p.Asn977Ser) rs1555482808
NM_001134407.3(GRIN2A):c.294C>T (p.Leu98=) rs771068226
NM_001134407.3(GRIN2A):c.2958T>G (p.Leu986=) rs1057522359
NM_001134407.3(GRIN2A):c.3030C>T (p.Pro1010=) rs763891276
NM_001134407.3(GRIN2A):c.3032G>T (p.Arg1011Leu) rs1163766811
NM_001134407.3(GRIN2A):c.3064C>A (p.Arg1022Ser) rs560057284
NM_001134407.3(GRIN2A):c.3178G>A (p.Asp1060Asn) rs879255358
NM_001134407.3(GRIN2A):c.3246C>G (p.Thr1082=) rs143039009
NM_001134407.3(GRIN2A):c.3387C>T (p.His1129=) rs1223085313
NM_001134407.3(GRIN2A):c.3391G>T (p.Asp1131Tyr) rs1243412120
NM_001134407.3(GRIN2A):c.3468A>T (p.Glu1156Asp) rs778180100
NM_001134407.3(GRIN2A):c.3492G>A (p.Thr1164=) rs1330743809
NM_001134407.3(GRIN2A):c.3544G>T (p.Asp1182Tyr) rs375160358
NM_001134407.3(GRIN2A):c.3553A>G (p.Lys1185Glu) rs587780354
NM_001134407.3(GRIN2A):c.3712G>A (p.Ala1238Thr) rs2141129928
NM_001134407.3(GRIN2A):c.3882C>T (p.Asn1294=) rs1057522011
NM_001134407.3(GRIN2A):c.3914G>C (p.Ser1305Thr)
NM_001134407.3(GRIN2A):c.4011G>A (p.Ser1337=) rs748586367
NM_001134407.3(GRIN2A):c.4081C>G (p.His1361Asp) rs797045606
NM_001134407.3(GRIN2A):c.415-15T>C rs1057522859
NM_001134407.3(GRIN2A):c.415G>T (p.Asp139Tyr) rs1555455852
NM_001134407.3(GRIN2A):c.420G>A (p.Pro140=) rs367543126
NM_001134407.3(GRIN2A):c.422C>T (p.Thr141Met) rs78631453
NM_001134407.3(GRIN2A):c.4235G>C (p.Cys1412Ser) rs1900675462
NM_001134407.3(GRIN2A):c.468G>T (p.Thr156=) rs773513210
NM_001134407.3(GRIN2A):c.822G>A (p.Ser274=) rs759344136
NM_001134407.3(GRIN2A):c.990G>T (p.Pro330=) rs149902963

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.