ClinVar Miner

List of variants in gene GRIN2B reported by Institute of Human Genetics, University of Leipzig Medical Center

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Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP gnomAD frequency
NM_000834.5(GRIN2B):c.1088del (p.Val363fs) rs1950068369
NM_000834.5(GRIN2B):c.1119G>A (p.Trp373Ter) rs1555119408
NM_000834.5(GRIN2B):c.1238A>G (p.Glu413Gly) rs527236034
NM_000834.5(GRIN2B):c.1306T>C (p.Cys436Arg) rs1565478152
NM_000834.5(GRIN2B):c.1367G>A (p.Cys456Tyr) rs397514555
NM_000834.5(GRIN2B):c.1382G>T (p.Cys461Phe) rs1949427787
NM_000834.5(GRIN2B):c.1495G>A (p.Gly499Arg) rs867553974
NM_000834.5(GRIN2B):c.1496G>T (p.Gly499Val) rs1949425904
NM_000834.5(GRIN2B):c.1500+1G>A
NM_000834.5(GRIN2B):c.1540A>G (p.Thr514Ala) rs1949421055
NM_000834.5(GRIN2B):c.1547A>G (p.Asn516Ser) rs886041295
NM_000834.5(GRIN2B):c.1573T>G (p.Phe525Val) rs1949420397
NM_000834.5(GRIN2B):c.1619G>A (p.Arg540His) rs672601378
NM_000834.5(GRIN2B):c.1623C>G (p.Ser541Arg) rs1949419853
NM_000834.5(GRIN2B):c.1648T>C (p.Phe550Leu)
NM_000834.5(GRIN2B):c.1658C>T (p.Pro553Leu) rs397514556
NM_000834.5(GRIN2B):c.1664G>T (p.Ser555Ile) rs1949369220
NM_000834.5(GRIN2B):c.1672G>A (p.Val558Ile) rs1057519004
NM_000834.5(GRIN2B):c.1677G>A (p.Trp559Ter) rs398122825
NM_000834.5(GRIN2B):c.1685T>C (p.Met562Thr) rs1949368766
NM_000834.5(GRIN2B):c.1700T>G (p.Leu567Arg)
NM_000834.5(GRIN2B):c.1821G>T (p.Trp607Cys) rs1057518700
NM_000834.5(GRIN2B):c.1832G>T (p.Gly611Val) rs1555110843
NM_000834.5(GRIN2B):c.1844A>T (p.Asn615Ile) rs672601377
NM_000834.5(GRIN2B):c.1845C>G (p.Asn615Lys) rs1949321538
NM_000834.5(GRIN2B):c.1848C>G (p.Asn616Lys) rs1949321461
NM_000834.5(GRIN2B):c.1853T>G (p.Val618Gly) rs672601376
NM_000834.5(GRIN2B):c.1858G>A (p.Val620Met) rs796052571
NM_000834.5(GRIN2B):c.1883C>G (p.Ser628Cys) rs1949320966
NM_000834.5(GRIN2B):c.1883C>T (p.Ser628Phe) rs1949320966
NM_000834.5(GRIN2B):c.1906G>C (p.Ala636Pro) rs1949320812
NM_000834.5(GRIN2B):c.1907C>T (p.Ala636Val) rs1555110818
NM_000834.5(GRIN2B):c.1916C>T (p.Ala639Val) rs797044930
NM_000834.5(GRIN2B):c.1963A>T (p.Ile655Phe) rs1949320223
NM_000834.5(GRIN2B):c.1966C>T (p.Gln656Ter) rs1135401799
NM_000834.5(GRIN2B):c.1970A>G (p.Glu657Gly) rs876661041
NM_000834.5(GRIN2B):c.1985A>C (p.Gln662Pro) rs1949319877
NM_000834.5(GRIN2B):c.2002G>T (p.Asp668Tyr) rs876661151
NM_000834.5(GRIN2B):c.2010G>A (p.Lys670=) rs1369104116
NM_000834.5(GRIN2B):c.2044C>T (p.Arg682Cys) rs387906636
NM_000834.5(GRIN2B):c.2060C>G (p.Pro687Arg) rs1555103986
NM_000834.5(GRIN2B):c.2060C>T (p.Pro687Leu) rs1555103986
NM_000834.5(GRIN2B):c.2065G>A (p.Gly689Ser)
NM_000834.5(GRIN2B):c.2079A>T (p.Arg693Ser) rs1948713322
NM_000834.5(GRIN2B):c.2084T>C (p.Ile695Thr) rs876661219
NM_000834.5(GRIN2B):c.2087G>A (p.Arg696His) rs1555103971
NM_000834.5(GRIN2B):c.2116A>G (p.Met706Val) rs1057518988
NM_000834.5(GRIN2B):c.2131C>T (p.Gln711Ter) rs1555103959
NM_000834.5(GRIN2B):c.2172-2A>G rs398122824
NM_000834.5(GRIN2B):c.2197G>C (p.Ala733Pro) rs2136413399
NM_000834.5(GRIN2B):c.2201C>T (p.Ala734Val) rs876661064
NM_000834.5(GRIN2B):c.2252T>C (p.Ile751Thr) rs876661055
NM_000834.5(GRIN2B):c.2360-2A>G rs1057519612
NM_000834.5(GRIN2B):c.2419G>A (p.Glu807Lys) rs1948652687
NM_000834.5(GRIN2B):c.2429G>A (p.Ser810Asn) rs1591609136
NM_000834.5(GRIN2B):c.2430C>A (p.Ser810Arg) rs864309560
NM_000834.5(GRIN2B):c.2452A>C (p.Met818Leu) rs876661076
NM_000834.5(GRIN2B):c.2453T>C (p.Met818Thr) rs879254016
NM_000834.5(GRIN2B):c.2455G>A (p.Ala819Thr) rs1948652117
NM_000834.5(GRIN2B):c.2459G>A (p.Gly820Glu) rs797044849
NM_000834.5(GRIN2B):c.2459G>C (p.Gly820Ala) rs797044849
NM_000834.5(GRIN2B):c.2459G>T (p.Gly820Val) rs797044849
NM_000834.5(GRIN2B):c.2470A>G (p.Met824Val)
NM_000834.5(GRIN2B):c.2471T>G (p.Met824Arg) rs1565455878
NM_000834.5(GRIN2B):c.2473T>G (p.Leu825Val) rs1948651813
NM_000834.5(GRIN2B):c.2477G>A (p.Gly826Glu) rs1064794979
NM_000834.5(GRIN2B):c.2510T>C (p.Ile837Thr) rs1565455844
NM_000834.5(GRIN2B):c.2539C>T (p.Arg847Ter) rs879253931
NM_000834.5(GRIN2B):c.2589del (p.Ile864fs) rs796052578
NM_000834.5(GRIN2B):c.2926_2928del (p.Lys976del) rs876661102
NM_000834.5(GRIN2B):c.3012C>G (p.Tyr1004Ter) rs201439880
NM_000834.5(GRIN2B):c.3295del (p.Arg1099fs) rs1948594989
NM_000834.5(GRIN2B):c.3332G>A (p.Arg1111His) rs876661167
NM_000834.5(GRIN2B):c.411+1G>A rs1057519611
NM_000834.5(GRIN2B):c.448A>G (p.Ile150Val) rs796052570
NM_000834.5(GRIN2B):c.538C>T (p.Gln180Ter) rs1555133154
NM_000834.5(GRIN2B):c.649C>T (p.Gln217Ter) rs1555133111
NM_000834.5(GRIN2B):c.718A>G (p.Ile240Val) rs2136629212
NM_000834.5(GRIN2B):c.737C>A (p.Ser246Ter) rs1863527228
NM_000834.5(GRIN2B):c.803_804del (p.Thr268fs) rs1060499526
NM_000834.5(GRIN2B):c.99dup (p.Ser34fs) rs398122823

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