ClinVar Miner

List of variants in gene GRIN2B reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 62
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HGVS dbSNP gnomAD frequency
NM_000834.5(GRIN2B):c.366C>G (p.Pro122=) rs7301328 0.41972
NM_000834.5(GRIN2B):c.3534C>T (p.His1178=) rs1806191 0.39095
NM_000834.5(GRIN2B):c.1665C>T (p.Ser555=) rs1805482 0.26553
NM_000834.5(GRIN2B):c.2664C>T (p.Thr888=) rs1806201 0.23527
NM_000834.5(GRIN2B):c.4197T>C (p.His1399=) rs1805247 0.16667
NM_000834.5(GRIN2B):c.2514C>T (p.Cys838=) rs3026160 0.08178
NM_000834.5(GRIN2B):c.15G>A (p.Ala5=) rs34315573 0.03193
NM_000834.5(GRIN2B):c.870C>T (p.Pro290=) rs1124894 0.02647
NM_000834.5(GRIN2B):c.504C>A (p.Ile168=) rs36031537 0.01733
NM_000834.5(GRIN2B):c.2691C>T (p.Asn897=) rs35125534 0.01112
NM_000834.5(GRIN2B):c.2599-19C>A rs3751258 0.00017
NM_000834.5(GRIN2B):c.1704C>T (p.Ile568=) rs202102041 0.00016
NM_000834.5(GRIN2B):c.189C>T (p.Ser63=) rs199707487 0.00016
NM_000834.5(GRIN2B):c.-12G>A rs201343005 0.00013
NM_000834.5(GRIN2B):c.2172-6G>A rs201390691 0.00010
NM_000834.5(GRIN2B):c.4311C>T (p.Ala1437=) rs112265127 0.00009
NM_000834.5(GRIN2B):c.2017A>C (p.Arg673=) rs149279923 0.00006
NM_000834.5(GRIN2B):c.1500+7G>A rs201094275 0.00005
NM_000834.5(GRIN2B):c.2359+16G>A rs781365670 0.00005
NM_000834.5(GRIN2B):c.3714G>T (p.Ala1238=) rs760725802 0.00004
NM_000834.5(GRIN2B):c.3993G>A (p.Met1331Ile) rs200035225 0.00004
NM_000834.5(GRIN2B):c.4179C>T (p.Asp1393=) rs199529615 0.00004
NM_000834.5(GRIN2B):c.327C>G (p.Ala109=) rs748395100 0.00003
NM_000834.5(GRIN2B):c.4107C>T (p.Gly1369=) rs201732760 0.00003
NM_000834.5(GRIN2B):c.51C>T (p.Ala17=) rs145404836 0.00003
NM_000834.5(GRIN2B):c.96C>A (p.Pro32=) rs374173060 0.00003
NM_000834.5(GRIN2B):c.1881C>T (p.Thr627=) rs768296067 0.00002
NM_000834.5(GRIN2B):c.4105G>A (p.Gly1369Ser) rs371190262 0.00002
NM_000834.5(GRIN2B):c.52G>A (p.Val18Ile) rs201094029 0.00002
NM_000834.5(GRIN2B):c.1501-19C>T rs377609698 0.00001
NM_000834.5(GRIN2B):c.1560G>A (p.Ser520=) rs566776310 0.00001
NM_000834.5(GRIN2B):c.1654+10G>A rs201242368 0.00001
NM_000834.5(GRIN2B):c.3660C>G (p.Ser1220=) rs201983807 0.00001
NM_000834.5(GRIN2B):c.3981G>A (p.Lys1327=) rs201670483 0.00001
NM_000834.5(GRIN2B):c.4014C>T (p.His1338=) rs758288071 0.00001
NM_000834.5(GRIN2B):c.4102G>A (p.Gly1368Ser) rs1043559346 0.00001
NM_000834.5(GRIN2B):c.412-14T>C rs879254251 0.00001
NM_000834.5(GRIN2B):c.4235C>A (p.Ala1412Glu) rs1314346300 0.00001
NM_000834.5(GRIN2B):c.4322G>A (p.Arg1441His) rs200903876 0.00001
NM_000834.5(GRIN2B):c.4413G>A (p.Gly1471=) rs202051424 0.00001
NM_000834.5(GRIN2B):c.519C>G (p.Thr173=) rs200357530 0.00001
NM_000834.5(GRIN2B):c.60C>T (p.Ala20=) rs371566007 0.00001
NM_000834.5(GRIN2B):c.1080G>T (p.Pro360=) rs201952040
NM_000834.5(GRIN2B):c.1099C>T (p.Leu367=) rs1057522928
NM_000834.5(GRIN2B):c.1704C>A (p.Ile568=) rs202102041
NM_000834.5(GRIN2B):c.1806C>T (p.Ile602=) rs1805522
NM_000834.5(GRIN2B):c.2011-20_2011-17del rs751965360
NM_000834.5(GRIN2B):c.2046C>G (p.Arg682=) rs1057522130
NM_000834.5(GRIN2B):c.2172-10del rs761900678
NM_000834.5(GRIN2B):c.2172-20_2172-17del rs765274847
NM_000834.5(GRIN2B):c.2360-15C>A rs1555103197
NM_000834.5(GRIN2B):c.2599-19C>T
NM_000834.5(GRIN2B):c.3195C>A (p.Thr1065=) rs879254211
NM_000834.5(GRIN2B):c.3339G>T (p.Pro1113=) rs200660626
NM_000834.5(GRIN2B):c.3456C>A (p.Thr1152=) rs752200554
NM_000834.5(GRIN2B):c.3751C>T (p.Leu1251=) rs200186058
NM_000834.5(GRIN2B):c.3819G>A (p.Thr1273=) rs1555101910
NM_000834.5(GRIN2B):c.3966A>G (p.Val1322=) rs1555101821
NM_000834.5(GRIN2B):c.444A>G (p.Pro148=) rs200658883
NM_000834.5(GRIN2B):c.540G>A (p.Gln180=) rs1057523105
NM_000834.5(GRIN2B):c.80G>T (p.Arg27Leu) rs200727145
NM_000834.5(GRIN2B):c.813G>A (p.Ala271=) rs201732785

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