ClinVar Miner

List of variants in gene GRIN2B reported as uncertain significance for not specified

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Gene type:
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Total variants: 28
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HGVS dbSNP
NM_000834.4(GRIN2B):c.1147T>A (p.Ser383Thr) rs199671864
NM_000834.4(GRIN2B):c.1479C>G (p.Thr493=) rs202139349
NM_000834.4(GRIN2B):c.1500+7G>A rs201094275
NM_000834.4(GRIN2B):c.1672G>A (p.Val558Ile) rs1057519004
NM_000834.4(GRIN2B):c.1851C>T (p.Ser617=) rs147373250
NM_000834.4(GRIN2B):c.1946A>C (p.Asn649Thr) rs879253945
NM_000834.4(GRIN2B):c.1946A>G (p.Asn649Ser) rs879253945
NM_000834.4(GRIN2B):c.2453T>C (p.Met818Thr) rs879254016
NM_000834.4(GRIN2B):c.248C>T (p.Thr83Ile) rs797045607
NM_000834.4(GRIN2B):c.2530T>C (p.Trp844Arg) rs138088984
NM_000834.4(GRIN2B):c.2810A>G (p.His937Arg) rs1168893427
NM_000834.4(GRIN2B):c.291G>A (p.Val97=) rs202223470
NM_000834.4(GRIN2B):c.2931C>G (p.Asp977Glu) rs147956755
NM_000834.4(GRIN2B):c.3076G>A (p.Gly1026Ser) rs201963596
NM_000834.4(GRIN2B):c.3499G>A (p.Val1167Ile) rs1042339
NM_000834.4(GRIN2B):c.3510A>T (p.Gly1170=) rs1555102142
NM_000834.4(GRIN2B):c.3626G>A (p.Arg1209Gln) rs748005909
NM_000834.4(GRIN2B):c.3703G>A (p.Gly1235Ser) rs886049099
NM_000834.4(GRIN2B):c.3747C>T (p.Gly1249=) rs138771137
NM_000834.4(GRIN2B):c.377T>C (p.Ile126Thr) rs879254008
NM_000834.4(GRIN2B):c.3964G>A (p.Val1322Ile) rs200255226
NM_000834.4(GRIN2B):c.4077C>T (p.Ala1359=) rs375217280
NM_000834.4(GRIN2B):c.4084_4086CAC[2] (p.His1364del) rs1214837315
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.4288G>C (p.Val1430Leu) rs879253885
NM_000834.4(GRIN2B):c.4309G>A (p.Ala1437Thr) rs797045608
NM_000834.4(GRIN2B):c.61G>A (p.Val21Met) rs79046967

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