ClinVar Miner

List of variants in gene GRIN2A reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 92
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HGVS dbSNP
NM_000833.5(GRIN2A):c.*3018G>C rs562770874
NM_000833.5(GRIN2A):c.*3341T>C rs576585646
NM_000833.5(GRIN2A):c.*3753C>G rs78426284
NM_000833.5(GRIN2A):c.*4281A>G rs570250938
NM_000833.5(GRIN2A):c.*4304T>C rs79079877
NM_000833.5(GRIN2A):c.*5076G>C rs182876220
NM_000833.5(GRIN2A):c.*5112C>T rs553874602
NM_000833.5(GRIN2A):c.*525G>A rs11575877
NM_000833.5(GRIN2A):c.*5365G>A rs554155423
NM_000833.5(GRIN2A):c.*6449G>T rs140145510
NM_000833.5(GRIN2A):c.*6846C>T rs566418840
NM_000833.5(GRIN2A):c.*7112A>T rs143274147
NM_000833.5(GRIN2A):c.*7650_*7654del rs537062402
NM_000833.5(GRIN2A):c.*9278C>T rs139007678
NM_000833.5(GRIN2A):c.*9325G>C rs117836220
NM_000833.5(GRIN2A):c.3246C>T (p.Thr1082=) rs143039009
NM_000833.5(GRIN2A):c.3427G>A (p.Glu1143Lys) rs61758996
NM_000833.5(GRIN2A):c.3884T>C (p.Ile1295Thr) rs757351084
NM_000833.5(GRIN2A):c.843C>T (p.Tyr281=) rs554338361
NM_001134407.3(GRIN2A):c.*1463C>T rs567206005
NM_001134407.3(GRIN2A):c.*1474T>C rs144327233
NM_001134407.3(GRIN2A):c.*1684A>C rs117255813
NM_001134407.3(GRIN2A):c.*2210A>T rs148482120
NM_001134407.3(GRIN2A):c.*2236G>A rs147419689
NM_001134407.3(GRIN2A):c.*2396G>A rs113138480
NM_001134407.3(GRIN2A):c.*2924A>C rs77580194
NM_001134407.3(GRIN2A):c.*2975G>A rs115979840
NM_001134407.3(GRIN2A):c.*3220C>T rs192984749
NM_001134407.3(GRIN2A):c.*3305C>A rs149492540
NM_001134407.3(GRIN2A):c.*3483C>T rs137977249
NM_001134407.3(GRIN2A):c.*39G>A rs141956850
NM_001134407.3(GRIN2A):c.*4036A>G rs9921182
NM_001134407.3(GRIN2A):c.*4251C>T rs537753852
NM_001134407.3(GRIN2A):c.*490G>A rs9937910
NM_001134407.3(GRIN2A):c.*4919C>T rs79849427
NM_001134407.3(GRIN2A):c.*5045T>A rs148967966
NM_001134407.3(GRIN2A):c.*5423T>C rs570847684
NM_001134407.3(GRIN2A):c.*5447G>T rs145736101
NM_001134407.3(GRIN2A):c.*5512T>C rs149933070
NM_001134407.3(GRIN2A):c.*5733C>T rs574207711
NM_001134407.3(GRIN2A):c.*5740A>C rs144545983
NM_001134407.3(GRIN2A):c.*5775T>A rs9933772
NM_001134407.3(GRIN2A):c.*5942G>A rs16966255
NM_001134407.3(GRIN2A):c.*5996C>T rs548588993
NM_001134407.3(GRIN2A):c.*6282T>A rs16966252
NM_001134407.3(GRIN2A):c.*6323C>T rs148431972
NM_001134407.3(GRIN2A):c.*6444G>A rs149410193
NM_001134407.3(GRIN2A):c.*6452G>A rs74011019
NM_001134407.3(GRIN2A):c.*6475T>A rs78377517
NM_001134407.3(GRIN2A):c.*6545C>A rs59394706
NM_001134407.3(GRIN2A):c.*6596C>T rs375205206
NM_001134407.3(GRIN2A):c.*6597G>A rs115306961
NM_001134407.3(GRIN2A):c.*6601G>C rs565650930
NM_001134407.3(GRIN2A):c.*6661G>A rs185399319
NM_001134407.3(GRIN2A):c.*6906T>G rs17791953
NM_001134407.3(GRIN2A):c.*6941C>T rs181271617
NM_001134407.3(GRIN2A):c.*6986A>G rs190006327
NM_001134407.3(GRIN2A):c.*722G>A rs569360567
NM_001134407.3(GRIN2A):c.*7349C>T rs191366035
NM_001134407.3(GRIN2A):c.*7898A>G rs530398129
NM_001134407.3(GRIN2A):c.*8077T>G rs16966243
NM_001134407.3(GRIN2A):c.*8396T>C rs192548671
NM_001134407.3(GRIN2A):c.*8536_*8537insC rs59371229
NM_001134407.3(GRIN2A):c.*8753T>C rs182174522
NM_001134407.3(GRIN2A):c.*9517T>C rs16966242
NM_001134407.3(GRIN2A):c.*9632T>A rs114596802
NM_001134407.3(GRIN2A):c.*9692A>G rs58340432
NM_001134407.3(GRIN2A):c.-220C>T rs139646156
NM_001134407.3(GRIN2A):c.-34C>A rs564039694
NM_001134407.3(GRIN2A):c.1652-13T>C rs201444481
NM_001134407.3(GRIN2A):c.2190C>T (p.Tyr730=) rs61753382
NM_001134407.3(GRIN2A):c.225C>T (p.Asn75=) rs527686036
NM_001134407.3(GRIN2A):c.2478C>T (p.Ala826=) rs373628160
NM_001134407.3(GRIN2A):c.2664G>A (p.Thr888=) rs113847665
NM_001134407.3(GRIN2A):c.2694C>T (p.Leu898=) rs569998469
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.2899G>C (p.Val967Leu) rs61731465
NM_001134407.3(GRIN2A):c.3064C>T (p.Arg1022Cys) rs560057284
NM_001134407.3(GRIN2A):c.3190A>G (p.Thr1064Ala) rs138809301
NM_001134407.3(GRIN2A):c.3228C>A (p.Asn1076Lys) rs61758995
NM_001134407.3(GRIN2A):c.3622C>A (p.Arg1208=) rs78544202
NM_001134407.3(GRIN2A):c.3702C>T (p.Phe1234=) rs372083517
NM_001134407.3(GRIN2A):c.3827C>G (p.Ala1276Gly) rs145063086
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.662A>G (p.Lys221Arg) rs61731464
NM_001134407.3(GRIN2A):c.819A>G (p.Pro273=) rs148085725
NM_001134407.3(GRIN2A):c.83A>C (p.Glu28Ala) rs146839931
NM_001134407.3(GRIN2A):c.900C>T (p.Thr300=) rs143669998
NM_001134407.3(GRIN2A):c.903C>T (p.Thr301=) rs78241448

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