ClinVar Miner

List of variants in gene GRIN2B reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_000834.5(GRIN2B):c.1341C>T (p.Asp447=) rs35025065 0.00902
NM_000834.5(GRIN2B):c.4240G>T (p.Ala1414Ser) rs140744818 0.00085
NM_000834.5(GRIN2B):c.1780+8C>T rs199986080 0.00068
NM_000834.5(GRIN2B):c.3747C>T (p.Gly1249=) rs138771137 0.00063
NM_000834.5(GRIN2B):c.3389G>A (p.Arg1130Gln) rs148625092 0.00043
NM_000834.5(GRIN2B):c.4101C>T (p.Pro1367=) rs112932810 0.00043
NM_000834.5(GRIN2B):c.812C>T (p.Ala271Val) rs138098032 0.00041
NM_000834.5(GRIN2B):c.3807A>T (p.Pro1269=) rs78765966 0.00035
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.1781-3C>T rs201520798 0.00010
NM_000834.5(GRIN2B):c.3957G>A (p.Pro1319=) rs141730031 0.00009
NM_000834.5(GRIN2B):c.3493G>A (p.Asp1165Asn) rs769857006 0.00008
NM_000834.5(GRIN2B):c.2628G>A (p.Ala876=) rs199710029 0.00007
NM_000834.5(GRIN2B):c.1768G>A (p.Ala590Thr) rs145021339 0.00006
NM_000834.5(GRIN2B):c.2001C>T (p.Ser667=) rs200392452 0.00006
NM_000834.5(GRIN2B):c.3818C>A (p.Thr1273Lys) rs531747728 0.00006
NM_000834.5(GRIN2B):c.275G>A (p.Arg92Gln) rs201966022 0.00004
NM_000834.5(GRIN2B):c.61G>A (p.Val21Met) rs79046967 0.00004
NM_000834.5(GRIN2B):c.1125G>A (p.Arg375=) rs200126922 0.00003
NM_000834.5(GRIN2B):c.1126-9C>T
NM_000834.5(GRIN2B):c.1378T>G (p.Phe460Val)
NM_000834.5(GRIN2B):c.1556G>A (p.Arg519Gln)
NM_000834.5(GRIN2B):c.1760G>A (p.Arg587Lys)
NM_000834.5(GRIN2B):c.216C>T (p.Ala72=)
NM_000834.5(GRIN2B):c.2172-10del rs761900678
NM_000834.5(GRIN2B):c.2459G>T (p.Gly820Val) rs797044849
NM_000834.5(GRIN2B):c.2530T>A (p.Trp844Arg)
NM_000834.5(GRIN2B):c.2806G>T (p.Glu936Ter)
NM_000834.5(GRIN2B):c.3201C>A (p.Thr1067=)
NM_000834.5(GRIN2B):c.4114A>G (p.Met1372Val)
NM_000834.5(GRIN2B):c.4288G>A (p.Val1430Met)
NM_000834.5(GRIN2B):c.845A>G (p.Tyr282Cys)

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