ClinVar Miner

List of variants in gene GRIN2B reported by Revvity Omics, Revvity

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Gene type:
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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_000834.5(GRIN2B):c.2931C>G (p.Asp977Glu) rs147956755 0.00029
NM_000834.5(GRIN2B):c.3076G>A (p.Gly1026Ser) rs201963596 0.00011
NM_000834.5(GRIN2B):c.3047G>A (p.Arg1016Lys) rs141109968 0.00006
NM_000834.5(GRIN2B):c.2648T>C (p.Val883Ala) rs770464893 0.00004
NM_000834.5(GRIN2B):c.136G>A (p.Asp46Asn) rs370809599 0.00001
NM_000834.5(GRIN2B):c.3099C>G (p.Ser1033Arg) rs796052575 0.00001
NM_000834.5(GRIN2B):c.4049C>T (p.Ala1350Val) rs763372245 0.00001
NM_000834.5(GRIN2B):c.4112A>G (p.Tyr1371Cys) rs755797497 0.00001
NM_000834.5(GRIN2B):c.4244C>T (p.Ser1415Leu) rs201463390 0.00001
NM_000834.5(GRIN2B):c.1288A>C (p.Met430Leu)
NM_000834.5(GRIN2B):c.1427A>G (p.Tyr476Cys)
NM_000834.5(GRIN2B):c.1705G>A (p.Val569Ile) rs1293991066
NM_000834.5(GRIN2B):c.200G>A (p.Arg67Gln)
NM_000834.5(GRIN2B):c.2010+1del rs2136470202
NM_000834.5(GRIN2B):c.2311G>C (p.Gly771Arg)
NM_000834.5(GRIN2B):c.2452A>T (p.Met818Leu)
NM_000834.5(GRIN2B):c.2487G>A (p.Met829Ile)
NM_000834.5(GRIN2B):c.2773A>G (p.Ile925Val)
NM_000834.5(GRIN2B):c.324C>T (p.Ile108=)
NM_000834.5(GRIN2B):c.3326A>G (p.Tyr1109Cys) rs1948594046
NM_000834.5(GRIN2B):c.3329G>A (p.Arg1110His) rs1271239566
NM_000834.5(GRIN2B):c.3372G>A (p.Arg1124=)
NM_000834.5(GRIN2B):c.3408G>C (p.Gln1136His)
NM_000834.5(GRIN2B):c.38G>T (p.Trp13Leu) rs765133670
NM_000834.5(GRIN2B):c.4244C>G (p.Ser1415Trp)
NM_000834.5(GRIN2B):c.4299C>T (p.Ala1433=)
NM_000834.5(GRIN2B):c.4374CAA[1] (p.Asn1459del)
NM_000834.5(GRIN2B):c.4409A>G (p.Asn1470Ser)
NM_000834.5(GRIN2B):c.544T>G (p.Phe182Val)
NM_000834.5(GRIN2B):c.805G>C (p.Val269Leu)
NM_000834.5(GRIN2B):c.857A>G (p.Asp286Gly)
NM_000834.5(GRIN2B):c.94C>A (p.Pro32Thr)

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