ClinVar Miner

List of variants in gene GRIN2B reported as benign

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Gene type:
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Total variants: 54
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HGVS dbSNP
NM_000834.4(GRIN2B):c.-15G>A rs12818068
NM_000834.4(GRIN2B):c.-18-10G>C rs146841522
NM_000834.4(GRIN2B):c.1035G>A (p.Glu345=) rs146812769
NM_000834.4(GRIN2B):c.1125+20A>G rs11055581
NM_000834.4(GRIN2B):c.1126-12A>G rs76777620
NM_000834.4(GRIN2B):c.1328+17A>G rs201560542
NM_000834.4(GRIN2B):c.1338A>G (p.Thr446=) rs141031272
NM_000834.4(GRIN2B):c.1341C>T (p.Asp447=) rs35025065
NM_000834.4(GRIN2B):c.140A>G (p.Glu47Gly) rs199526748
NM_000834.4(GRIN2B):c.1501-13G>A rs201829637
NM_000834.4(GRIN2B):c.1501-97C>T
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.1780+8C>T rs199986080
NM_000834.4(GRIN2B):c.1780+9G>A rs201461091
NM_000834.4(GRIN2B):c.1806C>T (p.Ile602=) rs1805522
NM_000834.4(GRIN2B):c.1851C>T (p.Ser617=) rs147373250
NM_000834.4(GRIN2B):c.2172-10delT rs761900678
NM_000834.4(GRIN2B):c.2172-176A>G
NM_000834.4(GRIN2B):c.2172-299T>C
NM_000834.4(GRIN2B):c.2202A>G (p.Ala734=) rs148185805
NM_000834.4(GRIN2B):c.228C>T (p.Thr76=) rs77299791
NM_000834.4(GRIN2B):c.2359+129A>G
NM_000834.4(GRIN2B):c.2359+224A>C
NM_000834.4(GRIN2B):c.2359+47C>A
NM_000834.4(GRIN2B):c.2360-225T>C
NM_000834.4(GRIN2B):c.2514C>T (p.Cys838=) rs3026160
NM_000834.4(GRIN2B):c.2628G>A (p.Ala876=) rs199710029
NM_000834.4(GRIN2B):c.2664C>T (p.Thr888=) rs1806201
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.291G>A (p.Val97=) rs202223470
NM_000834.4(GRIN2B):c.2975A>G (p.His992Arg) rs1555102461
NM_000834.4(GRIN2B):c.3117C>T (p.Tyr1039=) rs147762014
NM_000834.4(GRIN2B):c.3498C>T (p.Ser1166=) rs45600931
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.3747C>T (p.Gly1249=) rs138771137
NM_000834.4(GRIN2B):c.3799G>T (p.Ala1267Ser) rs141844705
NM_000834.4(GRIN2B):c.3807A>T (p.Pro1269=) rs78765966
NM_000834.4(GRIN2B):c.3837T>G (p.Thr1279=) rs1806200
NM_000834.4(GRIN2B):c.4077C>T (p.Ala1359=) rs375217280
NM_000834.4(GRIN2B):c.4105G>A (p.Gly1369Ser) rs371190262
NM_000834.4(GRIN2B):c.4113C>T (p.Tyr1371=) rs146792012
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.4311C>T (p.Ala1437=) rs112265127
NM_000834.4(GRIN2B):c.45G>A (p.Val15=) rs374735893
NM_000834.4(GRIN2B):c.465C>A (p.Ser155=) rs115189840
NM_000834.4(GRIN2B):c.504C>A (p.Ile168=) rs36031537
NM_000834.4(GRIN2B):c.771C>T (p.Ile257=) rs142203984
NM_000834.4(GRIN2B):c.870C>T (p.Pro290=) rs1124894

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