ClinVar Miner

List of variants in gene GRIN2A reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 75
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HGVS dbSNP
NM_000833.5(GRIN2A):c.*1002C>T rs144997779
NM_000833.5(GRIN2A):c.*7324G>A rs16966244
NM_000833.5(GRIN2A):c.447G>A (p.Ala149=) rs144464666
NM_001134407.3(GRIN2A):c.*1212C>T rs1014531
NM_001134407.3(GRIN2A):c.*121G>T rs75272984
NM_001134407.3(GRIN2A):c.*1385C>A rs113843373
NM_001134407.3(GRIN2A):c.*2017C>G rs112151383
NM_001134407.3(GRIN2A):c.*2617G>C rs62034910
NM_001134407.3(GRIN2A):c.*2803A>G rs16966263
NM_001134407.3(GRIN2A):c.*3721T>C rs16966262
NM_001134407.3(GRIN2A):c.*4739T>C rs111346223
NM_001134407.3(GRIN2A):c.*5776A>T rs78296872
NM_001134407.3(GRIN2A):c.*5818C>T rs8044472
NM_001134407.3(GRIN2A):c.*5884G>A rs8045712
NM_001134407.3(GRIN2A):c.*6128A>G rs9933624
NM_001134407.3(GRIN2A):c.*6149C>G rs9940680
NM_001134407.3(GRIN2A):c.*6609T>C rs1420040
NM_001134407.3(GRIN2A):c.*8535A>C rs767749
NM_001134407.3(GRIN2A):c.*8978G>C rs79818496
NM_001134407.3(GRIN2A):c.-18-345C>A
NM_001134407.3(GRIN2A):c.-19+8C>T rs563518225
NM_001134407.3(GRIN2A):c.-220C>T rs139646156
NM_001134407.3(GRIN2A):c.-34C>A rs564039694
NM_001134407.3(GRIN2A):c.1008-16C>G rs9932916
NM_001134407.3(GRIN2A):c.1122+133T>C
NM_001134407.3(GRIN2A):c.1122+320G>A
NM_001134407.3(GRIN2A):c.1123-177T>C
NM_001134407.3(GRIN2A):c.1251C>A (p.Val417=) rs139329447
NM_001134407.3(GRIN2A):c.1251C>T (p.Val417=) rs139329447
NM_001134407.3(GRIN2A):c.1275G>A (p.Leu425=) rs2229193
NM_001134407.3(GRIN2A):c.1328+142A>T
NM_001134407.3(GRIN2A):c.1328+181C>A
NM_001134407.3(GRIN2A):c.1329-105A>C
NM_001134407.3(GRIN2A):c.1329-272A>G
NM_001134407.3(GRIN2A):c.1329-317del
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.1410T>G (p.Thr470=) rs372058698
NM_001134407.3(GRIN2A):c.1629C>T (p.Thr543=) rs758378272
NM_001134407.3(GRIN2A):c.1652-13T>C rs201444481
NM_001134407.3(GRIN2A):c.1652-14C>G rs375922984
NM_001134407.3(GRIN2A):c.1777+17G>A rs375869375
NM_001134407.3(GRIN2A):c.1777+6G>T rs76549675
NM_001134407.3(GRIN2A):c.2007+101C>T
NM_001134407.3(GRIN2A):c.2007+15C>T rs76627672
NM_001134407.3(GRIN2A):c.2007+16T>C rs371738664
NM_001134407.3(GRIN2A):c.2008-14C>T rs375126711
NM_001134407.3(GRIN2A):c.2008-32CT[6]
NM_001134407.3(GRIN2A):c.2085G>C (p.Arg695=) rs9806806
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.2277C>T (p.Thr759=) rs148846694
NM_001134407.3(GRIN2A):c.2325C>T (p.Ile775=) rs748291723
NM_001134407.3(GRIN2A):c.2357-247C>A
NM_001134407.3(GRIN2A):c.2595+152C>A
NM_001134407.3(GRIN2A):c.2694C>T (p.Leu898=) rs569998469
NM_001134407.3(GRIN2A):c.2760A>G (p.Arg920=) rs80138441
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.306C>T (p.Asp102=) rs200850130
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.415-309G>A
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.662A>G (p.Lys221Arg) rs61731464
NM_001134407.3(GRIN2A):c.669C>T (p.His223=) rs138117658
NM_001134407.3(GRIN2A):c.819A>G (p.Pro273=) rs148085725
NM_001134407.3(GRIN2A):c.882C>T (p.Asp294=) rs201002710
NM_001134407.3(GRIN2A):c.900C>T (p.Thr300=) rs143669998
NM_001134407.3(GRIN2A):c.903C>T (p.Thr301=) rs78241448
NM_001134407.3(GRIN2A):c.939C>T (p.Ile313=) rs146867324

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