ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 126
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HGVS dbSNP gnomAD frequency
NM_000834.5(GRIN2B):c.2011-197T>C rs74538624 0.03019
NM_000834.5(GRIN2B):c.1010+308C>T rs141963477 0.01504
NM_000834.5(GRIN2B):c.1011-271C>T rs78753740 0.01119
NM_000834.5(GRIN2B):c.2360-153T>C rs112509252 0.01116
NM_000834.5(GRIN2B):c.2172-63G>A rs112785244 0.01115
NM_000834.5(GRIN2B):c.411+293C>T rs140139395 0.01110
NM_000834.5(GRIN2B):c.2010+25C>T rs115140153 0.00857
NM_000834.5(GRIN2B):c.1780+133C>T rs11055542 0.00622
NM_000834.5(GRIN2B):c.-18-10G>C rs146841522 0.00215
NM_000834.5(GRIN2B):c.3552C>T (p.Gly1184=) rs141886903 0.00206
NM_000834.5(GRIN2B):c.*1230G>C rs151270374 0.00172
NM_000834.5(GRIN2B):c.228C>T (p.Thr76=) rs77299791 0.00070
NM_000834.5(GRIN2B):c.2599-29T>C rs202079946 0.00037
NM_000834.5(GRIN2B):c.3807A>T (p.Pro1269=) rs78765966 0.00035
NM_000834.5(GRIN2B):c.3799G>T (p.Ala1267Ser) rs141844705 0.00029
NM_000834.5(GRIN2B):c.4113C>T (p.Tyr1371=) rs146792012 0.00029
NM_000834.5(GRIN2B):c.3413G>A (p.Arg1138Gln) rs187979330 0.00025
NM_000834.5(GRIN2B):c.1356C>T (p.Tyr452=) rs142935139 0.00023
NM_000834.5(GRIN2B):c.2813G>A (p.Arg938His) rs150445188 0.00019
NM_000834.5(GRIN2B):c.1500+47C>T rs182836140 0.00018
NM_000834.5(GRIN2B):c.189C>T (p.Ser63=) rs199707487 0.00016
NM_000834.5(GRIN2B):c.3648C>T (p.Arg1216=) rs201405157 0.00016
NM_000834.5(GRIN2B):c.2481G>A (p.Ala827=) rs189384622 0.00015
NM_000834.5(GRIN2B):c.2712G>A (p.Thr904=) rs199843136 0.00014
NM_000834.5(GRIN2B):c.190G>A (p.Val64Met) rs150070901 0.00011
NM_000834.5(GRIN2B):c.3076G>A (p.Gly1026Ser) rs201963596 0.00011
NM_000834.5(GRIN2B):c.2172-6G>A rs201390691 0.00010
NM_000834.5(GRIN2B):c.1654+36G>A rs562716391 0.00009
NM_000834.5(GRIN2B):c.2808G>A (p.Glu936=) rs77493389 0.00009
NM_000834.5(GRIN2B):c.4311C>T (p.Ala1437=) rs112265127 0.00009
NM_000834.5(GRIN2B):c.140A>G (p.Glu47Gly) rs199526748 0.00008
NM_000834.5(GRIN2B):c.513C>T (p.Ile171=) rs3026183 0.00008
NM_000834.5(GRIN2B):c.1023T>C (p.Asn341=) rs201228929 0.00007
NM_000834.5(GRIN2B):c.1275G>A (p.Leu425=) rs950679024 0.00007
NM_000834.5(GRIN2B):c.2172-4A>G rs367915298 0.00007
NM_000834.5(GRIN2B):c.99C>A (p.Pro33=) rs77738206 0.00007
NM_000834.5(GRIN2B):c.1768G>A (p.Ala590Thr) rs145021339 0.00006
NM_000834.5(GRIN2B):c.3047G>A (p.Arg1016Lys) rs141109968 0.00006
NM_000834.5(GRIN2B):c.3797C>T (p.Pro1266Leu) rs201947553 0.00006
NM_000834.5(GRIN2B):c.3818C>A (p.Thr1273Lys) rs531747728 0.00006
NM_000834.5(GRIN2B):c.1500+7G>A rs201094275 0.00005
NM_000834.5(GRIN2B):c.1780+19G>A rs201169461 0.00005
NM_000834.5(GRIN2B):c.1875G>C (p.Gly625=) rs201095094 0.00005
NM_000834.5(GRIN2B):c.514G>A (p.Val172Ile) rs201377003 0.00005
NM_000834.5(GRIN2B):c.975C>T (p.His325=) rs200380868 0.00005
NM_000834.5(GRIN2B):c.170A>T (p.Asp57Val) rs1019298480 0.00004
NM_000834.5(GRIN2B):c.2247G>A (p.Val749=) rs757990373 0.00004
NM_000834.5(GRIN2B):c.2648T>C (p.Val883Ala) rs770464893 0.00004
NM_000834.5(GRIN2B):c.2661C>A (p.Pro887=) rs201157664 0.00004
NM_000834.5(GRIN2B):c.2826G>A (p.Thr942=) rs140573925 0.00004
NM_000834.5(GRIN2B):c.282C>A (p.Ile94=) rs147132902 0.00004
NM_000834.5(GRIN2B):c.2910C>T (p.Phe970=) rs201252525 0.00004
NM_000834.5(GRIN2B):c.3000C>T (p.Ile1000=) rs772837930 0.00004
NM_000834.5(GRIN2B):c.3812C>T (p.Ala1271Val) rs372379846 0.00004
NM_000834.5(GRIN2B):c.4194C>T (p.Leu1398=) rs201247892 0.00004
NM_000834.5(GRIN2B):c.61G>A (p.Val21Met) rs79046967 0.00004
NM_000834.5(GRIN2B):c.630C>T (p.Asp210=) rs202115787 0.00004
NM_000834.5(GRIN2B):c.1125G>A (p.Arg375=) rs200126922 0.00003
NM_000834.5(GRIN2B):c.1316G>A (p.Arg439His) rs752720799 0.00003
NM_000834.5(GRIN2B):c.2644T>G (p.Ser882Ala) rs145602964 0.00003
NM_000834.5(GRIN2B):c.3300G>A (p.Arg1100=) rs200509787 0.00003
NM_000834.5(GRIN2B):c.3837T>G (p.Thr1279=) rs1806200 0.00003
NM_000834.5(GRIN2B):c.3922G>A (p.Val1308Met) rs374746622 0.00003
NM_000834.5(GRIN2B):c.3945C>T (p.Ala1315=) rs200657400 0.00003
NM_000834.5(GRIN2B):c.51C>T (p.Ala17=) rs145404836 0.00003
NM_000834.5(GRIN2B):c.6G>A (p.Lys2=) rs1346810637 0.00003
NM_000834.5(GRIN2B):c.2055C>T (p.Thr685=) rs375843467 0.00002
NM_000834.5(GRIN2B):c.2359+16G>C rs781365670 0.00002
NM_000834.5(GRIN2B):c.3285G>A (p.Ser1095=) rs200058641 0.00002
NM_000834.5(GRIN2B):c.4066G>A (p.Val1356Met) rs796052579 0.00002
NM_000834.5(GRIN2B):c.4241C>T (p.Ala1414Val) rs751107971 0.00002
NM_000834.5(GRIN2B):c.4410T>C (p.Asn1470=) rs199819153 0.00002
NM_000834.5(GRIN2B):c.732C>G (p.Ala244=) rs201554036 0.00002
NM_000834.5(GRIN2B):c.1125+19A>C rs181390006 0.00001
NM_000834.5(GRIN2B):c.138C>T (p.Asp46=) rs200527066 0.00001
NM_000834.5(GRIN2B):c.2250C>G (p.Thr750=) rs752150199 0.00001
NM_000834.5(GRIN2B):c.2637G>A (p.Glu879=) rs200754384 0.00001
NM_000834.5(GRIN2B):c.3081C>A (p.Leu1027=) rs200887288 0.00001
NM_000834.5(GRIN2B):c.3111C>A (p.Asp1037Glu) rs754878801 0.00001
NM_000834.5(GRIN2B):c.370C>T (p.Leu124=) rs780865592 0.00001
NM_000834.5(GRIN2B):c.381C>T (p.His127=) rs200608452 0.00001
NM_000834.5(GRIN2B):c.3981G>A (p.Lys1327=) rs201670483 0.00001
NM_000834.5(GRIN2B):c.4049C>T (p.Ala1350Val) rs763372245 0.00001
NM_000834.5(GRIN2B):c.4245G>A (p.Ser1415=) rs150956675 0.00001
NM_000834.5(GRIN2B):c.4375A>G (p.Asn1459Asp) rs1384338205 0.00001
NM_000834.5(GRIN2B):c.447A>T (p.Ser149=) rs1309787373 0.00001
NM_000834.5(GRIN2B):c.519C>G (p.Thr173=) rs200357530 0.00001
NM_000834.5(GRIN2B):c.991C>A (p.Gln331Lys) rs1290922060 0.00001
NM_000834.5(GRIN2B):c.999T>C (p.Asn333=) rs779643614 0.00001
NM_000834.5(GRIN2B):c.-47G>T rs199499610
NM_000834.5(GRIN2B):c.1038G>A (p.Gly346=) rs753955843
NM_000834.5(GRIN2B):c.1125+86C>A rs150976312
NM_000834.5(GRIN2B):c.1147T>A (p.Ser383Thr) rs199671864
NM_000834.5(GRIN2B):c.1176C>A (p.Pro392=) rs1555112397
NM_000834.5(GRIN2B):c.1449T>C (p.Asn483=)
NM_000834.5(GRIN2B):c.1479C>A (p.Thr493=) rs202139349
NM_000834.5(GRIN2B):c.1479C>T (p.Thr493=)
NM_000834.5(GRIN2B):c.153G>A (p.Lys51=) rs1057522391
NM_000834.5(GRIN2B):c.1620C>T (p.Arg540=) rs1591642598
NM_000834.5(GRIN2B):c.1655-12dup rs768388356
NM_000834.5(GRIN2B):c.1739T>A (p.Phe580Tyr) rs199801114
NM_000834.5(GRIN2B):c.2040T>C (p.Pro680=) rs1948713794
NM_000834.5(GRIN2B):c.2172-6G>T
NM_000834.5(GRIN2B):c.2172G>T (p.Gly724=) rs200813905
NM_000834.5(GRIN2B):c.2202A>C (p.Ala734=) rs148185805
NM_000834.5(GRIN2B):c.2457A>G (p.Ala819=)
NM_000834.5(GRIN2B):c.253A>G (p.Ile85Val)
NM_000834.5(GRIN2B):c.2856G>A (p.Pro952=) rs547507161
NM_000834.5(GRIN2B):c.2997C>T (p.Ser999=)
NM_000834.5(GRIN2B):c.3099C>T (p.Ser1033=)
NM_000834.5(GRIN2B):c.3213G>A (p.Gly1071=) rs1591606576
NM_000834.5(GRIN2B):c.3339G>A (p.Pro1113=) rs200660626
NM_000834.5(GRIN2B):c.351A>G (p.Ala117=) rs1230018548
NM_000834.5(GRIN2B):c.3588T>A (p.Pro1196=) rs200884387
NM_000834.5(GRIN2B):c.366C>A (p.Pro122=) rs7301328
NM_000834.5(GRIN2B):c.3753G>T (p.Leu1251=) rs748973212
NM_000834.5(GRIN2B):c.3759C>T (p.Asp1253=)
NM_000834.5(GRIN2B):c.3819G>A (p.Thr1273=) rs1555101910
NM_000834.5(GRIN2B):c.411+151del rs1025093263
NM_000834.5(GRIN2B):c.4287G>A (p.Pro1429=) rs146235271
NM_000834.5(GRIN2B):c.4309G>A (p.Ala1437Thr) rs797045608
NM_000834.5(GRIN2B):c.465C>T (p.Ser155=) rs115189840
NM_000834.5(GRIN2B):c.618C>T (p.Asp206=)
NM_000834.5(GRIN2B):c.812C>A (p.Ala271Glu) rs138098032
NM_000834.5(GRIN2B):c.831C>T (p.Leu277=)
NM_000834.5(GRIN2B):c.846T>C (p.Tyr282=) rs1208230861

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