ClinVar Miner

List of variants in gene GRIN2B reported as likely pathogenic for not provided

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Gene type:
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Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_000834.5(GRIN2B):c.1555C>T (p.Arg519Ter) rs774592932 0.00001
NM_000834.5(GRIN2B):c.1016del (p.Leu339fs) rs1950069601
NM_000834.5(GRIN2B):c.1456C>T (p.His486Tyr) rs2136479935
NM_000834.5(GRIN2B):c.1495G>A (p.Gly499Arg) rs867553974
NM_000834.5(GRIN2B):c.1744C>T (p.Pro582Ser)
NM_000834.5(GRIN2B):c.1858G>A (p.Val620Met) rs796052571
NM_000834.5(GRIN2B):c.1946A>G (p.Asn649Ser) rs879253945
NM_000834.5(GRIN2B):c.1955C>G (p.Ala652Gly) rs879253912
NM_000834.5(GRIN2B):c.1963A>G (p.Ile655Val) rs1949320223
NM_000834.5(GRIN2B):c.1970A>G (p.Glu657Gly) rs876661041
NM_000834.5(GRIN2B):c.2001C>A (p.Ser667Arg) rs200392452
NM_000834.5(GRIN2B):c.2002G>T (p.Asp668Tyr) rs876661151
NM_000834.5(GRIN2B):c.2026G>A (p.Asp676Asn) rs1565457924
NM_000834.5(GRIN2B):c.2084T>G (p.Ile695Ser) rs876661219
NM_000834.5(GRIN2B):c.2116A>G (p.Met706Val) rs1057518988
NM_000834.5(GRIN2B):c.2189T>C (p.Ile730Thr) rs1948686554
NM_000834.5(GRIN2B):c.2201C>T (p.Ala734Val) rs876661064
NM_000834.5(GRIN2B):c.2238C>G (p.Cys746Trp) rs941763104
NM_000834.5(GRIN2B):c.2251A>C (p.Ile751Leu) rs879254013
NM_000834.5(GRIN2B):c.2450A>G (p.Asn817Ser) rs1555103159
NM_000834.5(GRIN2B):c.2452A>C (p.Met818Leu) rs876661076
NM_000834.5(GRIN2B):c.2452A>T (p.Met818Leu)
NM_000834.5(GRIN2B):c.2455G>T (p.Ala819Ser) rs1948652117
NM_000834.5(GRIN2B):c.2458G>A (p.Gly820Arg) rs1555103150
NM_000834.5(GRIN2B):c.2486dup (p.Met829fs) rs1591609065
NM_000834.5(GRIN2B):c.2515G>A (p.Glu839Lys) rs1085307547
NM_000834.5(GRIN2B):c.2539C>T (p.Arg847Ter) rs879253931
NM_000834.5(GRIN2B):c.2557_2558del (p.Val853fs) rs876661022
NM_000834.5(GRIN2B):c.2589del (p.Ile864fs) rs796052578
NM_000834.5(GRIN2B):c.2599-1G>A
NM_000834.5(GRIN2B):c.2674_2698dup (p.Arg900fs) rs2136406273
NM_000834.5(GRIN2B):c.2750C>T (p.Ser917Leu) rs1555102552
NM_000834.5(GRIN2B):c.2926_2928del (p.Lys976del) rs876661102
NM_000834.5(GRIN2B):c.3006_3009dup (p.Tyr1004fs) rs1057518520
NM_000834.5(GRIN2B):c.3301G>T (p.Glu1101Ter) rs1555102308
NM_000834.5(GRIN2B):c.3332G>A (p.Arg1111His) rs876661167
NM_000834.5(GRIN2B):c.3915dup (p.Thr1306fs) rs1591605549
NM_000834.5(GRIN2B):c.4015_4016del (p.Met1339fs) rs1565453023
NM_000834.5(GRIN2B):c.4244del (p.Ala1414_Ser1415insTer) rs1948569124
NM_000834.5(GRIN2B):c.99dup (p.Ser34fs) rs398122823

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