ClinVar Miner

List of variants in gene GRIN2A reported by Invitae

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Gene type:
ClinVar version:
Total variants: 146
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HGVS dbSNP
NC_000016.10:g.(?_10179978)_(10180431_?)dup
NC_000016.10:g.(?_9849736)_(9849981_?)del
NC_000016.10:g.(?_9890966)_(9891120_?)del
NC_000016.9:g.(?_10273835)_(10274288_?)del
NM_000833.4(GRIN2A):c.1007+1G>A rs397518465
NM_000833.4(GRIN2A):c.1008-9C>G rs111844068
NM_000833.4(GRIN2A):c.1030G>C (p.Asp344His)
NM_000833.4(GRIN2A):c.1057G>A (p.Glu353Lys)
NM_000833.4(GRIN2A):c.1170G>T (p.Trp390Cys) rs1555496181
NM_000833.4(GRIN2A):c.1224C>T (p.Ile408=) rs776264780
NM_000833.4(GRIN2A):c.1249G>A (p.Val417Ile) rs749504561
NM_000833.4(GRIN2A):c.1251C>A (p.Val417=) rs139329447
NM_000833.4(GRIN2A):c.1251C>T (p.Val417=) rs139329447
NM_000833.4(GRIN2A):c.1323A>C (p.Lys441Asn)
NM_000833.4(GRIN2A):c.1329-8C>T rs7193290
NM_000833.4(GRIN2A):c.1329-9T>G rs541442732
NM_000833.4(GRIN2A):c.1354G>A (p.Val452Met) rs145956175
NM_000833.4(GRIN2A):c.1380C>T (p.Cys460=) rs375291296
NM_000833.4(GRIN2A):c.1382T>A (p.Ile461Asn)
NM_000833.4(GRIN2A):c.1458C>A (p.Gly486=) rs144572467
NM_000833.4(GRIN2A):c.1553G>A (p.Arg518His) rs397518470
NM_000833.4(GRIN2A):c.1553G>T (p.Arg518Leu)
NM_000833.4(GRIN2A):c.1629C>T (p.Thr543=) rs758378272
NM_000833.4(GRIN2A):c.1673G>C (p.Trp558Ser) rs1555493585
NM_000833.4(GRIN2A):c.1734C>G (p.Tyr578Ter) rs1060503228
NM_000833.4(GRIN2A):c.1777+6G>T rs76549675
NM_000833.4(GRIN2A):c.1780C>T (p.Pro594Ser) rs367543140
NM_000833.4(GRIN2A):c.179C>T (p.Ala60Val)
NM_000833.4(GRIN2A):c.1901G>A (p.Trp634Ter) rs1555492769
NM_000833.4(GRIN2A):c.2007+10C>T rs368110989
NM_000833.4(GRIN2A):c.2069C>T (p.Thr690Met) rs1445802934
NM_000833.4(GRIN2A):c.2165C>T (p.Thr722Met) rs376029542
NM_000833.4(GRIN2A):c.2190C>T (p.Tyr730=) rs61753382
NM_000833.4(GRIN2A):c.2197G>A (p.Ala733Thr) rs796052550
NM_000833.4(GRIN2A):c.225C>T (p.Asn75=) rs527686036
NM_000833.4(GRIN2A):c.2278G>A (p.Gly760Ser) rs1555488119
NM_000833.4(GRIN2A):c.2325C>T (p.Ile775=) rs748291723
NM_000833.4(GRIN2A):c.2346_2356+8delTGTGGGTGATGGTAAGACC rs1064795143
NM_000833.4(GRIN2A):c.2441T>C (p.Ile814Thr) rs780654733
NM_000833.4(GRIN2A):c.2445C>A (p.Asp815Glu)
NM_000833.4(GRIN2A):c.2452G>A (p.Ala818Thr) rs1555483699
NM_000833.4(GRIN2A):c.2505C>T (p.Phe835=) rs771342023
NM_000833.4(GRIN2A):c.2549C>T (p.Thr850Met) rs1060503230
NM_000833.4(GRIN2A):c.2563G>A (p.Asp855Asn) rs796052564
NM_000833.4(GRIN2A):c.258G>A (p.Val86=) rs774606054
NM_000833.4(GRIN2A):c.2627T>C (p.Ile876Thr) rs199784503
NM_000833.4(GRIN2A):c.2674A>G (p.Ser892Gly) rs1060503229
NM_000833.4(GRIN2A):c.2695C>T (p.Arg899Trp) rs796052553
NM_000833.4(GRIN2A):c.2735C>G (p.Ser912Cys) rs200588845
NM_000833.4(GRIN2A):c.2744T>C (p.Met915Thr) rs1060503231
NM_000833.4(GRIN2A):c.2749T>G (p.Ser917Ala) rs1060503232
NM_000833.4(GRIN2A):c.2760A>G (p.Arg920=) rs80138441
NM_000833.4(GRIN2A):c.2765C>T (p.Ala922Val) rs200037904
NM_000833.4(GRIN2A):c.2779A>G (p.Arg927Gly) rs761044372
NM_000833.4(GRIN2A):c.2805T>G (p.Val935=) rs762984731
NM_000833.4(GRIN2A):c.2811T>A (p.Asp937Glu) rs570907044
NM_000833.4(GRIN2A):c.2852G>T (p.Gly951Val) rs139795367
NM_000833.4(GRIN2A):c.2877C>T (p.Asn959=) rs756576680
NM_000833.4(GRIN2A):c.2883C>T (p.Asn961=) rs77705198
NM_000833.4(GRIN2A):c.288C>G (p.His96Gln) rs74853460
NM_000833.4(GRIN2A):c.288C>T (p.His96=) rs74853460
NM_000833.4(GRIN2A):c.2899G>C (p.Val967Leu) rs61731465
NM_000833.4(GRIN2A):c.2907C>G (p.Asn969Lys) rs772589363
NM_000833.4(GRIN2A):c.2966A>G (p.Asn989Ser) rs531782747
NM_000833.4(GRIN2A):c.2985G>C (p.Thr995=) rs781646325
NM_000833.4(GRIN2A):c.3003C>T (p.Ser1001=) rs199551487
NM_000833.4(GRIN2A):c.3039G>A (p.Leu1013=) rs577077724
NM_000833.4(GRIN2A):c.3042G>A (p.Trp1014Ter)
NM_000833.4(GRIN2A):c.306C>T (p.Asp102=) rs200850130
NM_000833.4(GRIN2A):c.3108G>A (p.Glu1036=) rs1555482675
NM_000833.4(GRIN2A):c.3176C>G (p.Ser1059Cys) rs772497745
NM_000833.4(GRIN2A):c.3190A>G (p.Thr1064Ala) rs138809301
NM_000833.4(GRIN2A):c.3211C>T (p.His1071Tyr) rs1555482611
NM_000833.4(GRIN2A):c.3228C>A (p.Asn1076Lys) rs61758995
NM_000833.4(GRIN2A):c.324C>T (p.Ala108=) rs762110435
NM_000833.4(GRIN2A):c.3293G>A (p.Cys1098Tyr) rs746257794
NM_000833.4(GRIN2A):c.3363T>G (p.Asp1121Glu) rs764292783
NM_000833.4(GRIN2A):c.3366T>G (p.Gly1122=) rs1060504864
NM_000833.4(GRIN2A):c.3391G>T (p.Asp1131Tyr)
NM_000833.4(GRIN2A):c.3400C>A (p.Gln1134Lys) rs748967552
NM_000833.4(GRIN2A):c.3468A>T (p.Glu1156Asp) rs778180100
NM_000833.4(GRIN2A):c.3476G>A (p.Arg1159His) rs534440095
NM_000833.4(GRIN2A):c.3505C>T (p.Arg1169Trp)
NM_000833.4(GRIN2A):c.3535T>G (p.Ser1179Ala) rs142670870
NM_000833.4(GRIN2A):c.3539A>T (p.Asn1180Ile) rs972229279
NM_000833.4(GRIN2A):c.3622C>A (p.Arg1208=) rs78544202
NM_000833.4(GRIN2A):c.3630C>T (p.Asn1210=) rs750892541
NM_000833.4(GRIN2A):c.3659A>C (p.Asn1220Thr) rs1131691913
NM_000833.4(GRIN2A):c.3687C>A (p.Thr1229=) rs1060504863
NM_000833.4(GRIN2A):c.3702C>T (p.Phe1234=) rs372083517
NM_000833.4(GRIN2A):c.3737A>G (p.Tyr1246Cys) rs779437393
NM_000833.4(GRIN2A):c.3820A>G (p.Asn1274Asp)
NM_000833.4(GRIN2A):c.3827C>G (p.Ala1276Gly) rs145063086
NM_000833.4(GRIN2A):c.3854G>A (p.Arg1285Lys) rs367543132
NM_000833.4(GRIN2A):c.3854G>T (p.Arg1285Met)
NM_000833.4(GRIN2A):c.38C>T (p.Pro13Leu) rs367543131
NM_000833.4(GRIN2A):c.3953G>A (p.Arg1318Gln) rs149745535
NM_000833.4(GRIN2A):c.3961G>C (p.Glu1321Gln) rs370754278
NM_000833.4(GRIN2A):c.402C>T (p.Ile134=) rs587780352
NM_000833.4(GRIN2A):c.4084A>G (p.Thr1362Ala) rs77282679
NM_000833.4(GRIN2A):c.4126C>T (p.Arg1376Cys) rs1426934537
NM_000833.4(GRIN2A):c.414+7C>T
NM_000833.4(GRIN2A):c.4140G>C (p.Gly1380=) rs373901698
NM_000833.4(GRIN2A):c.4176A>G (p.Pro1392=) rs886043681
NM_000833.4(GRIN2A):c.4185G>A (p.Ala1395=) rs778429009
NM_000833.4(GRIN2A):c.419C>T (p.Pro140Leu) rs142566406
NM_000833.4(GRIN2A):c.4205G>A (p.Arg1402Gln)
NM_000833.4(GRIN2A):c.422C>T (p.Thr141Met) rs78631453
NM_000833.4(GRIN2A):c.4230G>A (p.Ser1410=) rs762437402
NM_000833.4(GRIN2A):c.4245C>A (p.Asp1415Glu) rs777328885
NM_000833.4(GRIN2A):c.4247G>C (p.Ser1416Thr) rs377712891
NM_000833.4(GRIN2A):c.4259A>G (p.Asn1420Ser)
NM_000833.4(GRIN2A):c.4307A>G (p.Asn1436Ser) rs77029288
NM_000833.4(GRIN2A):c.4330G>A (p.Val1444Ile) rs150574045
NM_000833.4(GRIN2A):c.4355G>A (p.Arg1452His)
NM_000833.4(GRIN2A):c.4356C>G (p.Arg1452=) rs140093291
NM_000833.4(GRIN2A):c.4373C>G (p.Pro1458Arg) rs933017490
NM_000833.4(GRIN2A):c.468G>A (p.Thr156=) rs773513210
NM_000833.4(GRIN2A):c.487C>T (p.Gln163Ter) rs1057524089
NM_000833.4(GRIN2A):c.522C>A (p.Thr174=) rs771962690
NM_000833.4(GRIN2A):c.540C>T (p.Tyr180=) rs745815376
NM_000833.4(GRIN2A):c.559G>A (p.Val187Ile) rs751692867
NM_000833.4(GRIN2A):c.60T>C (p.Gly20=) rs367543130
NM_000833.4(GRIN2A):c.623C>T (p.Thr208Ile) rs367543124
NM_000833.4(GRIN2A):c.634G>A (p.Asp212Asn)
NM_000833.4(GRIN2A):c.63G>C (p.Pro21=) rs1060504865
NM_000833.4(GRIN2A):c.662A>G (p.Lys221Arg) rs61731464
NM_000833.4(GRIN2A):c.666C>T (p.Ile222=) rs143594020
NM_000833.4(GRIN2A):c.669C>T (p.His223=) rs138117658
NM_000833.4(GRIN2A):c.702C>T (p.Asp234=) rs150208429
NM_000833.4(GRIN2A):c.741C>T (p.Gly247=) rs141912603
NM_000833.4(GRIN2A):c.76G>T (p.Ala26Ser) rs751198815
NM_000833.4(GRIN2A):c.794C>T (p.Thr265Met)
NM_000833.4(GRIN2A):c.819A>G (p.Pro273=) rs148085725
NM_000833.4(GRIN2A):c.828C>G (p.Leu276=) rs752295285
NM_000833.4(GRIN2A):c.837C>G (p.Val279=) rs55885632
NM_000833.4(GRIN2A):c.882C>T (p.Asp294=) rs201002710
NM_000833.4(GRIN2A):c.883G>A (p.Gly295Ser) rs568484876
NM_000833.4(GRIN2A):c.886A>G (p.Ile296Val) rs953400144
NM_000833.4(GRIN2A):c.900C>T (p.Thr300=) rs143669998
NM_000833.4(GRIN2A):c.903C>T (p.Thr301=) rs78241448
NM_000833.4(GRIN2A):c.939C>T (p.Ile313=) rs146867324
NM_000833.4(GRIN2A):c.942C>T (p.Pro314=) rs145172949
NM_000833.4(GRIN2A):c.952G>A (p.Ala318Thr)
NM_000833.4(GRIN2A):c.963C>T (p.Tyr321=) rs368200727
NM_000833.4(GRIN2A):c.979C>G (p.Pro327Ala) rs771168389

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