ClinVar Miner

List of variants in gene GRIN2B reported as likely benign by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP
NM_000834.4(GRIN2B):c.1080G>A (p.Pro360=)
NM_000834.4(GRIN2B):c.1338A>G (p.Thr446=) rs141031272
NM_000834.4(GRIN2B):c.1356C>T (p.Tyr452=) rs142935139
NM_000834.4(GRIN2B):c.1560G>A (p.Ser520=) rs566776310
NM_000834.4(GRIN2B):c.1569C>T (p.Val523=) rs148573953
NM_000834.4(GRIN2B):c.1704C>A (p.Ile568=) rs202102041
NM_000834.4(GRIN2B):c.1851C>T (p.Ser617=) rs147373250
NM_000834.4(GRIN2B):c.2202A>G (p.Ala734=) rs148185805
NM_000834.4(GRIN2B):c.2247G>A (p.Val749=) rs757990373
NM_000834.4(GRIN2B):c.228C>T (p.Thr76=) rs77299791
NM_000834.4(GRIN2B):c.2481G>A (p.Ala827=) rs189384622
NM_000834.4(GRIN2B):c.2628G>A (p.Ala876=) rs199710029
NM_000834.4(GRIN2B):c.2703G>A (p.Leu901=) rs145005918
NM_000834.4(GRIN2B):c.2847C>T (p.Tyr949=) rs771565713
NM_000834.4(GRIN2B):c.2856G>A (p.Pro952=)
NM_000834.4(GRIN2B):c.291G>A (p.Val97=) rs202223470
NM_000834.4(GRIN2B):c.2991C>A (p.Ala997=)
NM_000834.4(GRIN2B):c.3006G>T (p.Gly1002=)
NM_000834.4(GRIN2B):c.3009C>G (p.Leu1003=) rs1460313772
NM_000834.4(GRIN2B):c.3076G>A (p.Gly1026Ser) rs201963596
NM_000834.4(GRIN2B):c.3117C>T (p.Tyr1039=) rs147762014
NM_000834.4(GRIN2B):c.3174C>T (p.Ser1058=) rs772364390
NM_000834.4(GRIN2B):c.3335G>A (p.Arg1112Gln)
NM_000834.4(GRIN2B):c.3504C>T (p.Ser1168=)
NM_000834.4(GRIN2B):c.3552C>T (p.Gly1184=) rs141886903
NM_000834.4(GRIN2B):c.3690G>A (p.Thr1230=)
NM_000834.4(GRIN2B):c.3747C>T (p.Gly1249=) rs138771137
NM_000834.4(GRIN2B):c.3837T>G (p.Thr1279=) rs1806200
NM_000834.4(GRIN2B):c.3945C>T (p.Ala1315=) rs200657400
NM_000834.4(GRIN2B):c.3993G>A (p.Met1331Ile) rs200035225
NM_000834.4(GRIN2B):c.4113C>T (p.Tyr1371=) rs146792012
NM_000834.4(GRIN2B):c.4240G>T (p.Ala1414Ser) rs140744818
NM_000834.4(GRIN2B):c.4269C>T (p.Ala1423=) rs1565452665
NM_000834.4(GRIN2B):c.4311C>T (p.Ala1437=) rs112265127
NM_000834.4(GRIN2B):c.513C>T (p.Ile171=) rs3026183
NM_000834.4(GRIN2B):c.812C>T (p.Ala271Val) rs138098032
NM_000834.4(GRIN2B):c.975C>T (p.His325=) rs200380868

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