ClinVar Miner

List of variants in gene GRIN2B studied for Mental retardation, autosomal dominant 6

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Total variants: 25
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HGVS dbSNP
NM_000834.4(GRIN2B):c.1238A>G (p.Glu413Gly) rs527236034
NM_000834.4(GRIN2B):c.1306T>C (p.Cys436Arg) rs1565478152
NM_000834.4(GRIN2B):c.1367G>A (p.Cys456Tyr) rs397514555
NM_000834.4(GRIN2B):c.1619G>A (p.Arg540His) rs672601378
NM_000834.4(GRIN2B):c.1658C>T (p.Pro553Leu) rs397514556
NM_000834.4(GRIN2B):c.1665C>T (p.Ser555=) rs1805482
NM_000834.4(GRIN2B):c.1677G>A (p.Trp559Ter) rs398122825
NM_000834.4(GRIN2B):c.1721_1726TCTTTG[1] (p.574_575VF[1]) rs1555111511
NM_000834.4(GRIN2B):c.1821G>C (p.Trp607Cys) rs1057518700
NM_000834.4(GRIN2B):c.1851C>T (p.Ser617=) rs147373250
NM_000834.4(GRIN2B):c.2044C>T (p.Arg682Cys) rs387906636
NM_000834.4(GRIN2B):c.2045G>A (p.Arg682His) rs886041095
NM_000834.4(GRIN2B):c.2065G>A (p.Gly689Ser) rs869312868
NM_000834.4(GRIN2B):c.2071A>G (p.Thr691Ala) rs1565457892
NM_000834.4(GRIN2B):c.2087G>A (p.Arg696His) rs1555103971
NM_000834.4(GRIN2B):c.2172-2A>G rs398122824
NM_000834.4(GRIN2B):c.2252T>C (p.Ile751Thr) rs876661055
NM_000834.4(GRIN2B):c.228C>T (p.Thr76=) rs77299791
NM_000834.4(GRIN2B):c.2360-2A>G rs1057519612
NM_000834.4(GRIN2B):c.2459G>C (p.Gly820Ala) rs797044849
NM_000834.4(GRIN2B):c.2471T>G (p.Met824Arg) rs1565455878
NM_000834.4(GRIN2B):c.3498C>T (p.Ser1166=) rs45600931
NM_000834.4(GRIN2B):c.411+1G>A rs1057519611
NM_000834.4(GRIN2B):c.801_802CA[1] (p.Thr268fs) rs1060499526
NM_000834.4(GRIN2B):c.99dup (p.Ser34fs) rs398122823

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