ClinVar Miner

List of variants in gene GRIN2B reported as uncertain significance by Ambry Genetics

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Gene type:
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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_000834.5(GRIN2B):c.3047G>A (p.Arg1016Lys) rs141109968 0.00006
NM_000834.5(GRIN2B):c.3473G>A (p.Arg1158Gln) rs143955920 0.00005
NM_000834.5(GRIN2B):c.170A>T (p.Asp57Val) rs1019298480 0.00004
NM_000834.5(GRIN2B):c.1125+5G>A rs3751257 0.00003
NM_000834.5(GRIN2B):c.2861G>A (p.Cys954Tyr) rs376328340 0.00003
NM_000834.5(GRIN2B):c.3922G>A (p.Val1308Met) rs374746622 0.00003
NM_000834.5(GRIN2B):c.80G>A (p.Arg27His) rs200727145 0.00003
NM_000834.5(GRIN2B):c.3499G>A (p.Val1167Ile) rs1042339 0.00002
NM_000834.5(GRIN2B):c.3884G>A (p.Arg1295Gln) rs1284336148 0.00002
NM_000834.5(GRIN2B):c.4066G>A (p.Val1356Met) rs796052579 0.00002
NM_000834.5(GRIN2B):c.241A>G (p.Ile81Val) rs200262227 0.00001
NM_000834.5(GRIN2B):c.274C>T (p.Arg92Trp) rs1436757161 0.00001
NM_000834.5(GRIN2B):c.2969G>A (p.Arg990Gln) rs1458162832 0.00001
NM_000834.5(GRIN2B):c.3652T>A (p.Cys1218Ser) rs1948583113 0.00001
NM_000834.5(GRIN2B):c.1394T>G (p.Leu465Arg)
NM_000834.5(GRIN2B):c.163G>A (p.Glu55Lys) rs763469464
NM_000834.5(GRIN2B):c.1922T>C (p.Ile641Thr) rs1949320609
NM_000834.5(GRIN2B):c.2011-5T>C rs2136416046
NM_000834.5(GRIN2B):c.2051G>A (p.Gly684Glu)
NM_000834.5(GRIN2B):c.2056G>A (p.Val686Met) rs2136415913
NM_000834.5(GRIN2B):c.2094C>G (p.Asn698Lys)
NM_000834.5(GRIN2B):c.2111C>T (p.Ala704Val) rs2136415760
NM_000834.5(GRIN2B):c.2138G>C (p.Gly713Ala)
NM_000834.5(GRIN2B):c.225G>C (p.Glu75Asp)
NM_000834.5(GRIN2B):c.2450A>G (p.Asn817Ser) rs1555103159
NM_000834.5(GRIN2B):c.2542C>T (p.His848Tyr)
NM_000834.5(GRIN2B):c.2598+1G>T
NM_000834.5(GRIN2B):c.2662A>G (p.Thr888Ala) rs200256539
NM_000834.5(GRIN2B):c.2810A>G (p.His937Arg) rs1168893427
NM_000834.5(GRIN2B):c.3232G>A (p.Ala1078Thr)
NM_000834.5(GRIN2B):c.3239G>A (p.Arg1080Lys)
NM_000834.5(GRIN2B):c.3416C>A (p.Thr1139Lys) rs1948591192
NM_000834.5(GRIN2B):c.3424A>G (p.Asn1142Asp)
NM_000834.5(GRIN2B):c.3491G>A (p.Arg1164His)
NM_000834.5(GRIN2B):c.3497C>G (p.Ser1166Cys)
NM_000834.5(GRIN2B):c.3539A>G (p.Lys1180Arg)
NM_000834.5(GRIN2B):c.3580C>T (p.Pro1194Ser)
NM_000834.5(GRIN2B):c.3601C>G (p.Leu1201Val) rs1434222109
NM_000834.5(GRIN2B):c.3670_3672del (p.Asn1224del) rs1555102005
NM_000834.5(GRIN2B):c.3806C>A (p.Pro1269Gln)
NM_000834.5(GRIN2B):c.3842A>G (p.Tyr1281Cys)
NM_000834.5(GRIN2B):c.396G>A (p.Met132Ile) rs1865817394
NM_000834.5(GRIN2B):c.3985C>G (p.Arg1329Gly) rs1555101805
NM_000834.5(GRIN2B):c.4096A>C (p.Asn1366His)
NM_000834.5(GRIN2B):c.4172T>C (p.Phe1391Ser) rs1948570623
NM_000834.5(GRIN2B):c.4316C>T (p.Pro1439Leu) rs1948566990
NM_000834.5(GRIN2B):c.80G>T (p.Arg27Leu) rs200727145
NM_000834.5(GRIN2B):c.817T>G (p.Phe273Val)
NM_000834.5(GRIN2B):c.845A>G (p.Tyr282Cys)
NM_000834.5(GRIN2B):c.992A>C (p.Gln331Pro)

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