ClinVar Miner

List of variants in gene GRIN2B studied for Intellectual Disability, Dominant

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Gene type:
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Total variants: 68
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HGVS dbSNP
NM_000834.3(GRIN2B):c.*1074C>T rs201335778
NM_000834.3(GRIN2B):c.*1153T>C rs145952835
NM_000834.3(GRIN2B):c.*1179C>T rs140845306
NM_000834.3(GRIN2B):c.*1230G>C rs151270374
NM_000834.3(GRIN2B):c.*146G>A rs886049097
NM_000834.3(GRIN2B):c.*214C>A rs200777193
NM_000834.3(GRIN2B):c.*219C>T rs80081965
NM_000834.3(GRIN2B):c.*368A>G rs1805504
NM_000834.3(GRIN2B):c.*409T>G rs890
NM_000834.3(GRIN2B):c.*891G>T rs201863953
NM_000834.3(GRIN2B):c.*951G>C rs886049094
NM_000834.3(GRIN2B):c.*988A>G rs1805477
NM_000834.3(GRIN2B):c.2169A>T (p.Thr723=) rs780117268
NM_000834.3(GRIN2B):c.2247G>A (p.Val749=) rs757990373
NM_000834.3(GRIN2B):c.2514C>T (p.Cys838=) rs3026160
NM_000834.3(GRIN2B):c.2664C>T (p.Thr888=) rs1806201
NM_000834.3(GRIN2B):c.2866G>A (p.Glu956Lys) rs886049101
NM_000834.3(GRIN2B):c.4041C>A (p.Ser1347Arg) rs769147604
NM_000834.3(GRIN2B):c.4113C>T (p.Tyr1371=) rs146792012
NM_000834.3(GRIN2B):c.4142G>A (p.Arg1381Gln) rs761443441
NM_000834.3(GRIN2B):c.4215C>T (p.Phe1405=) rs778677489
NM_000834.4(GRIN2B):c.*110_*113del rs886049098
NM_000834.4(GRIN2B):c.*1164A>G rs571293410
NM_000834.4(GRIN2B):c.*232T>C rs886049096
NM_000834.4(GRIN2B):c.*235T>A rs200812783
NM_000834.4(GRIN2B):c.*25_*28del rs751398824
NM_000834.4(GRIN2B):c.*285G>A rs71539419
NM_000834.4(GRIN2B):c.*293G>A rs199764468
NM_000834.4(GRIN2B):c.*30C>G rs759518484
NM_000834.4(GRIN2B):c.*342C>T rs78222734
NM_000834.4(GRIN2B):c.*567A>C rs1805503
NM_000834.4(GRIN2B):c.*862T>C rs886049095
NM_000834.4(GRIN2B):c.-15G>A rs12818068
NM_000834.4(GRIN2B):c.-18-10G>C rs146841522
NM_000834.4(GRIN2B):c.-9G>T rs748524822
NM_000834.4(GRIN2B):c.1126-12A>G rs76777620
NM_000834.4(GRIN2B):c.1320A>T (p.Ile440=) rs753284709
NM_000834.4(GRIN2B):c.1500G>A (p.Glu500=) rs886049102
NM_000834.4(GRIN2B):c.1569C>T (p.Val523=) rs148573953
NM_000834.4(GRIN2B):c.15G>A (p.Ala5=) rs34315573
NM_000834.4(GRIN2B):c.1665C>T (p.Ser555=) rs1805482
NM_000834.4(GRIN2B):c.1767C>T (p.Leu589=) rs763286576
NM_000834.4(GRIN2B):c.1768G>A (p.Ala590Thr) rs145021339
NM_000834.4(GRIN2B):c.1806C>T (p.Ile602=) rs1805522
NM_000834.4(GRIN2B):c.189C>T (p.Ser63=) rs199707487
NM_000834.4(GRIN2B):c.190G>A (p.Val64Met) rs150070901
NM_000834.4(GRIN2B):c.2172-8C>T rs751592819
NM_000834.4(GRIN2B):c.2481G>A (p.Ala827=) rs189384622
NM_000834.4(GRIN2B):c.2628G>A (p.Ala876=) rs199710029
NM_000834.4(GRIN2B):c.2691C>T (p.Asn897=) rs35125534
NM_000834.4(GRIN2B):c.2703G>A (p.Leu901=) rs145005918
NM_000834.4(GRIN2B):c.2826G>A (p.Thr942=) rs140573925
NM_000834.4(GRIN2B):c.2890A>G (p.Ser964Gly) rs886049100
NM_000834.4(GRIN2B):c.3174C>T (p.Ser1058=) rs772364390
NM_000834.4(GRIN2B):c.33G>A (p.Lys11=) rs199904091
NM_000834.4(GRIN2B):c.3534C>T (p.His1178=) rs1806191
NM_000834.4(GRIN2B):c.3552C>T (p.Gly1184=) rs141886903
NM_000834.4(GRIN2B):c.366C>G (p.Pro122=) rs7301328
NM_000834.4(GRIN2B):c.3703G>A (p.Gly1235Ser) rs886049099
NM_000834.4(GRIN2B):c.3807A>T (p.Pro1269=) rs78765966
NM_000834.4(GRIN2B):c.3825C>T (p.Asn1275=) rs200571186
NM_000834.4(GRIN2B):c.3837T>G (p.Thr1279=) rs1806200
NM_000834.4(GRIN2B):c.4197T>C (p.His1399=) rs1805247
NM_000834.4(GRIN2B):c.4218C>T (p.Phe1406=) rs1805246
NM_000834.4(GRIN2B):c.4230G>A (p.Thr1410=) rs149655315
NM_000834.4(GRIN2B):c.504C>A (p.Ile168=) rs36031537
NM_000834.4(GRIN2B):c.732C>G (p.Ala244=) rs201554036
NM_000834.4(GRIN2B):c.870C>T (p.Pro290=) rs1124894

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