ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 80
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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.1329-8C>T rs7193290 0.01998
NM_001134407.3(GRIN2A):c.2899G>C (p.Val967Leu) rs61731465 0.00502
NM_001134407.3(GRIN2A):c.662A>G (p.Lys221Arg) rs61731464 0.00322
NM_001134407.3(GRIN2A):c.903C>T (p.Thr301=) rs78241448 0.00119
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.2277C>T (p.Thr759=) rs148846694 0.00024
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.949A>C (p.Lys317Gln) rs141326581 0.00011
NM_001134407.3(GRIN2A):c.1007+13T>G rs199862009 0.00009
NM_001134407.3(GRIN2A):c.1652-19T>C rs778659119 0.00007
NM_001134407.3(GRIN2A):c.3898A>G (p.Arg1300Gly) rs372353067 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.3103G>A (p.Asp1035Asn) rs540445580 0.00006
NM_001134407.3(GRIN2A):c.4170G>A (p.Ser1390=) rs1057522803 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.2478C>T (p.Ala826=) rs373628160 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.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.1593G>A (p.Thr531=) rs957436270 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.3636G>A (p.Thr1212=) rs765614514 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.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_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.1428C>T (p.Asp476=) rs762674544
NM_001134407.3(GRIN2A):c.1498-11C>T rs759632014
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.2007+11C>G rs758596798
NM_001134407.3(GRIN2A):c.2049G>C (p.Gly683=) rs1057523027
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.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.3246C>G (p.Thr1082=) rs143039009
NM_001134407.3(GRIN2A):c.3387C>T (p.His1129=) rs1223085313
NM_001134407.3(GRIN2A):c.3492G>A (p.Thr1164=) rs1330743809
NM_001134407.3(GRIN2A):c.3553A>G (p.Lys1185Glu) rs587780354
NM_001134407.3(GRIN2A):c.3882C>T (p.Asn1294=) rs1057522011
NM_001134407.3(GRIN2A):c.4011G>A (p.Ser1337=) rs748586367
NM_001134407.3(GRIN2A):c.415-15T>C rs1057522859
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.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

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