ClinVar Miner

List of variants in gene GRIN2B reported as likely benign by Invitae

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Gene type:
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Total variants: 40
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HGVS dbSNP
NM_000834.4(GRIN2B):c.1023T>C (p.Asn341=) rs201228929
NM_000834.4(GRIN2B):c.138C>T (p.Asp46=) rs200527066
NM_000834.4(GRIN2B):c.144G>A (p.Val48=) rs201242152
NM_000834.4(GRIN2B):c.1704C>T (p.Ile568=) rs202102041
NM_000834.4(GRIN2B):c.174T>C (p.Asp58=) rs1555149549
NM_000834.4(GRIN2B):c.1878C>A (p.Thr626=) rs1555110827
NM_000834.4(GRIN2B):c.2017A>C (p.Arg673=) rs149279923
NM_000834.4(GRIN2B):c.2172-6G>A rs201390691
NM_000834.4(GRIN2B):c.2172-8C>T rs751592819
NM_000834.4(GRIN2B):c.2247G>A (p.Val749=) rs757990373
NM_000834.4(GRIN2B):c.2481G>A (p.Ala827=) rs189384622
NM_000834.4(GRIN2B):c.2715C>T (p.Ala905=) rs568858172
NM_000834.4(GRIN2B):c.2754G>A (p.Pro918=) rs756487785
NM_000834.4(GRIN2B):c.2847C>T (p.Tyr949=) rs771565713
NM_000834.4(GRIN2B):c.2913G>A (p.Gly971=) rs200696950
NM_000834.4(GRIN2B):c.291G>A (p.Val97=) rs202223470
NM_000834.4(GRIN2B):c.3078C>T (p.Gly1026=) rs1555102406
NM_000834.4(GRIN2B):c.3146A>G (p.Tyr1049Cys) rs201866998
NM_000834.4(GRIN2B):c.3174C>T (p.Ser1058=) rs772364390
NM_000834.4(GRIN2B):c.3275G>A (p.Arg1092Gln) rs1555102321
NM_000834.4(GRIN2B):c.3285G>A (p.Ser1095=) rs200058641
NM_000834.4(GRIN2B):c.3306T>C (p.Phe1102=) rs763445499
NM_000834.4(GRIN2B):c.3339G>A (p.Pro1113=) rs200660626
NM_000834.4(GRIN2B):c.336C>T (p.Leu112=) rs1060504845
NM_000834.4(GRIN2B):c.3389G>A (p.Arg1130Gln) rs148625092
NM_000834.4(GRIN2B):c.3648C>T (p.Arg1216=) rs201405157
NM_000834.4(GRIN2B):c.3807A>G (p.Pro1269=) rs78765966
NM_000834.4(GRIN2B):c.3807A>T (p.Pro1269=) rs78765966
NM_000834.4(GRIN2B):c.3957G>A (p.Pro1319=) rs141730031
NM_000834.4(GRIN2B):c.3981G>A (p.Lys1327=) rs201670483
NM_000834.4(GRIN2B):c.4240G>T (p.Ala1414Ser) rs140744818
NM_000834.4(GRIN2B):c.4296G>A (p.Ser1432=) rs755880051
NM_000834.4(GRIN2B):c.4416T>G (p.His1472Gln) rs1555101497
NM_000834.4(GRIN2B):c.513C>T (p.Ile171=) rs3026183
NM_000834.4(GRIN2B):c.519C>G (p.Thr173=) rs200357530
NM_000834.4(GRIN2B):c.61G>A (p.Val21Met) rs79046967
NM_000834.4(GRIN2B):c.681C>A (p.Ile227=) rs148254591
NM_000834.4(GRIN2B):c.732C>G (p.Ala244=) rs201554036
NM_000834.4(GRIN2B):c.765G>A (p.Thr255=) rs199844735
NM_000834.4(GRIN2B):c.975C>T (p.His325=) rs200380868

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