ClinVar Miner

Variants in gene GRIN2A with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 55
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HGVS dbSNP gnomAD frequency
NM_001134407.3(GRIN2A):c.1354G>A (p.Val452Met) rs145956175 0.00105
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.666C>T (p.Ile222=) rs143594020 0.00039
NM_001134407.3(GRIN2A):c.741C>T (p.Gly247=) rs141912603 0.00039
NM_001134407.3(GRIN2A):c.2165C>T (p.Thr722Met) rs376029542 0.00024
NM_001134407.3(GRIN2A):c.736C>A (p.Leu246Ile) rs555768104 0.00021
NM_001134407.3(GRIN2A):c.3535T>G (p.Ser1179Ala) rs142670870 0.00010
NM_001134407.3(GRIN2A):c.4330G>A (p.Val1444Ile) rs150574045 0.00008
NM_001134407.3(GRIN2A):c.4353A>T (p.Arg1451Ser) rs143693526 0.00008
NM_001134407.3(GRIN2A):c.3898A>G (p.Arg1300Gly) rs372353067 0.00007
NM_001134407.3(GRIN2A):c.2909G>A (p.Arg970Gln) rs148669437 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.2811T>A (p.Asp937Glu) rs570907044 0.00005
NM_001134407.3(GRIN2A):c.3505C>T (p.Arg1169Trp) rs369878342 0.00005
NM_001134407.3(GRIN2A):c.567C>A (p.Thr189=) rs758864728 0.00005
NM_001134407.3(GRIN2A):c.1119A>G (p.Glu373=) rs368406915 0.00004
NM_001134407.3(GRIN2A):c.2664G>A (p.Thr888=) rs113847665 0.00004
NM_001134407.3(GRIN2A):c.3363T>G (p.Asp1121Glu) rs764292783 0.00004
NM_001134407.3(GRIN2A):c.3787G>A (p.Gly1263Arg) rs142113044 0.00004
NM_001134407.3(GRIN2A):c.3884T>C (p.Ile1295Thr) rs757351084 0.00004
NM_001134407.3(GRIN2A):c.3961G>C (p.Glu1321Gln) rs370754278 0.00004
NM_001134407.3(GRIN2A):c.547T>A (p.Phe183Ile) rs587780353 0.00004
NM_001134407.3(GRIN2A):c.747C>T (p.Thr249=) rs774169125 0.00004
NM_001134407.3(GRIN2A):c.3578T>G (p.Leu1193Trp) rs75761674 0.00003
NM_001134407.3(GRIN2A):c.3854G>A (p.Arg1285Lys) rs367543132 0.00003
NM_001134407.3(GRIN2A):c.1380C>T (p.Cys460=) rs375291296 0.00002
NM_001134407.3(GRIN2A):c.2650G>A (p.Asp884Asn) rs777684328 0.00002
NM_001134407.3(GRIN2A):c.3338C>T (p.Pro1113Leu) rs201698049 0.00002
NM_001134407.3(GRIN2A):c.1030G>C (p.Asp344His) rs777505684 0.00001
NM_001134407.3(GRIN2A):c.1069G>A (p.Val357Met) rs78929970 0.00001
NM_001134407.3(GRIN2A):c.1343A>G (p.Glu448Gly) rs1273711716 0.00001
NM_001134407.3(GRIN2A):c.3017C>T (p.Ala1006Val) rs200526162 0.00001
NM_001134407.3(GRIN2A):c.3636G>A (p.Thr1212=) rs765614514 0.00001
NM_001134407.3(GRIN2A):c.3809A>T (p.Asp1270Val) rs750649530 0.00001
NM_001134407.3(GRIN2A):c.678C>T (p.Val226=) rs1567187672 0.00001
NM_001134407.3(GRIN2A):c.687C>T (p.Leu229=) rs372649219 0.00001
NM_001134407.3(GRIN2A):c.77C>T (p.Ala26Val) rs765986049 0.00001
NM_001134407.3(GRIN2A):c.843C>T (p.Tyr281=) rs554338361 0.00001
NM_001134407.3(GRIN2A):c.943G>A (p.Glu315Lys) rs765104792 0.00001
NM_001134407.3(GRIN2A):c.964G>A (p.Gly322Arg) rs374637415 0.00001
NM_001134407.3(GRIN2A):c.979C>G (p.Pro327Ala) rs771168389 0.00001
NM_001134407.3(GRIN2A):c.1074C>G (p.His358Gln) rs763315364
NM_001134407.3(GRIN2A):c.1777+6G>T rs76549675
NM_001134407.3(GRIN2A):c.2049G>C (p.Gly683=) rs1057523027
NM_001134407.3(GRIN2A):c.2494C>T (p.Leu832Phe) rs145495027
NM_001134407.3(GRIN2A):c.288C>G (p.His96Gln) rs74853460
NM_001134407.3(GRIN2A):c.3211C>T (p.His1071Tyr) rs1555482611
NM_001134407.3(GRIN2A):c.3544G>T (p.Asp1182Tyr) rs375160358
NM_001134407.3(GRIN2A):c.3668C>G (p.Thr1223Ser) rs770966136
NM_001134407.3(GRIN2A):c.3854G>T (p.Arg1285Met) rs367543132
NM_001134407.3(GRIN2A):c.4006C>T (p.Leu1336Phe)
NM_001134407.3(GRIN2A):c.67_81del (p.Pro23_Ala27del) rs775540481

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