ClinVar Miner

List of variants in gene GRIN2B reported as uncertain significance by GeneDx

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Total variants: 56
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HGVS dbSNP
NM_000834.4(GRIN2B):c.-10C>T rs200539507
NM_000834.4(GRIN2B):c.1125G>A (p.Arg375=) rs200126922
NM_000834.4(GRIN2B):c.1126-3C>T rs1555112424
NM_000834.4(GRIN2B):c.1147T>A (p.Ser383Thr) rs199671864
NM_000834.4(GRIN2B):c.125T>C (p.Val42Ala) rs796052580
NM_000834.4(GRIN2B):c.1316G>A (p.Arg439His) rs752720799
NM_000834.4(GRIN2B):c.140A>G (p.Glu47Gly) rs199526748
NM_000834.4(GRIN2B):c.1745C>G (p.Pro582Arg) rs796052581
NM_000834.4(GRIN2B):c.1946A>C (p.Asn649Thr) rs879253945
NM_000834.4(GRIN2B):c.2453T>C (p.Met818Thr) rs879254016
NM_000834.4(GRIN2B):c.251G>A (p.Arg84His) rs778695605
NM_000834.4(GRIN2B):c.2530T>C (p.Trp844Arg) rs138088984
NM_000834.4(GRIN2B):c.2555_2556GT[1] (p.Val853fs) rs876661022
NM_000834.4(GRIN2B):c.2662A>G (p.Thr888Ala) rs200256539
NM_000834.4(GRIN2B):c.2759G>A (p.Ser920Asn) rs781442804
NM_000834.4(GRIN2B):c.2931C>G (p.Asp977Glu) rs147956755
NM_000834.4(GRIN2B):c.2936A>T (p.Asn979Ile) rs796052574
NM_000834.4(GRIN2B):c.3047G>A (p.Arg1016Lys) rs141109968
NM_000834.4(GRIN2B):c.3056G>T (p.Ser1019Ile) rs200265732
NM_000834.4(GRIN2B):c.3076G>A (p.Gly1026Ser) rs201963596
NM_000834.4(GRIN2B):c.3099C>G (p.Ser1033Arg) rs796052575
NM_000834.4(GRIN2B):c.3137G>T (p.Ser1046Ile) rs201029083
NM_000834.4(GRIN2B):c.3170G>A (p.Arg1057His) rs773737239
NM_000834.4(GRIN2B):c.3200C>T (p.Thr1067Ile) rs1555102353
NM_000834.4(GRIN2B):c.3241C>A (p.Arg1081Ser) rs796052576
NM_000834.4(GRIN2B):c.325G>T (p.Ala109Ser) rs772078838
NM_000834.4(GRIN2B):c.3301G>T (p.Glu1101Ter) rs1555102308
NM_000834.4(GRIN2B):c.3413G>T (p.Arg1138Leu) rs187979330
NM_000834.4(GRIN2B):c.3499G>A (p.Val1167Ile) rs1042339
NM_000834.4(GRIN2B):c.3626G>A (p.Arg1209Gln) rs748005909
NM_000834.4(GRIN2B):c.36C>A (p.Phe12Leu) rs752668123
NM_000834.4(GRIN2B):c.3745G>T (p.Gly1249Cys) rs796052577
NM_000834.4(GRIN2B):c.377T>C (p.Ile126Thr) rs879254008
NM_000834.4(GRIN2B):c.3812C>T (p.Ala1271Val) rs372379846
NM_000834.4(GRIN2B):c.3883C>T (p.Arg1295Trp) rs560662030
NM_000834.4(GRIN2B):c.3893T>C (p.Leu1298Pro) rs876661100
NM_000834.4(GRIN2B):c.3922G>A (p.Val1308Met) rs374746622
NM_000834.4(GRIN2B):c.3964G>A (p.Val1322Ile) rs200255226
NM_000834.4(GRIN2B):c.4041C>A (p.Ser1347Arg) rs769147604
NM_000834.4(GRIN2B):c.4066G>A (p.Val1356Met) rs796052579
NM_000834.4(GRIN2B):c.4142G>A (p.Arg1381Gln) rs761443441
NM_000834.4(GRIN2B):c.4261T>C (p.Phe1421Leu) rs879254129
NM_000834.4(GRIN2B):c.4265G>A (p.Arg1422Gln) rs75269586
NM_000834.4(GRIN2B):c.4288G>C (p.Val1430Leu) rs879253885
NM_000834.4(GRIN2B):c.4292T>C (p.Val1431Ala) rs1555101581
NM_000834.4(GRIN2B):c.4312G>A (p.Val1438Met) rs763699668
NM_000834.4(GRIN2B):c.4355C>T (p.Ser1452Phe) rs756790727
NM_000834.4(GRIN2B):c.4400G>C (p.Gly1467Ala) rs200127692
NM_000834.4(GRIN2B):c.466G>A (p.Val156Ile) rs1555133189
NM_000834.4(GRIN2B):c.471G>C (p.Met157Ile) rs876661185
NM_000834.4(GRIN2B):c.61G>A (p.Val21Met) rs79046967
NM_000834.4(GRIN2B):c.679A>G (p.Ile227Val) rs201672517
NM_000834.4(GRIN2B):c.730G>T (p.Ala244Ser) rs1555133062
NM_000834.4(GRIN2B):c.841T>A (p.Ser281Thr) rs1085307651
NM_000834.4(GRIN2B):c.876A>G (p.Arg292=) rs876661173
NM_000834.4(GRIN2B):c.935G>A (p.Ser312Asn) rs1085307687

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