ClinVar Miner

List of variants in gene GRIN2B reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_000834.5(GRIN2B):c.3498C>T (p.Ser1166=) rs45600931 0.00538
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.3117C>T (p.Tyr1039=) rs147762014 0.00123
NM_000834.5(GRIN2B):c.228C>T (p.Thr76=) rs77299791 0.00070
NM_000834.5(GRIN2B):c.3747C>T (p.Gly1249=) rs138771137 0.00063
NM_000834.5(GRIN2B):c.1851C>T (p.Ser617=) rs147373250 0.00045
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.189C>T (p.Ser63=) rs199707487 0.00016
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.2808G>A (p.Glu936=) rs77493389 0.00009
NM_000834.5(GRIN2B):c.513C>T (p.Ile171=) rs3026183 0.00008
NM_000834.5(GRIN2B):c.1080G>A (p.Pro360=) rs201952040 0.00006
NM_000834.5(GRIN2B):c.1500+7G>A rs201094275 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.2247G>A (p.Val749=) rs757990373 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.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.1350G>A (p.Pro450=) rs200607718 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.51C>T (p.Ala17=) rs145404836 0.00003
NM_000834.5(GRIN2B):c.3285G>A (p.Ser1095=) rs200058641 0.00002
NM_000834.5(GRIN2B):c.4105G>A (p.Gly1369Ser) rs371190262 0.00002
NM_000834.5(GRIN2B):c.138C>T (p.Asp46=) rs200527066 0.00001
NM_000834.5(GRIN2B):c.1560G>A (p.Ser520=) rs566776310 0.00001
NM_000834.5(GRIN2B):c.327C>G (p.Ala109=) rs748395100 0.00001
NM_000834.5(GRIN2B):c.3981G>A (p.Lys1327=) rs201670483 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.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.2172-6G>T
NM_000834.5(GRIN2B):c.2202A>G (p.Ala734=) rs148185805
NM_000834.5(GRIN2B):c.2457A>G (p.Ala819=)
NM_000834.5(GRIN2B):c.2688C>A (p.Ser896=)
NM_000834.5(GRIN2B):c.2826G>T (p.Thr942=) rs140573925
NM_000834.5(GRIN2B):c.2856G>A (p.Pro952=) rs547507161
NM_000834.5(GRIN2B):c.288G>A (p.Gly96=)
NM_000834.5(GRIN2B):c.2997C>T (p.Ser999=)
NM_000834.5(GRIN2B):c.3099C>T (p.Ser1033=)
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.3759C>T (p.Asp1253=)
NM_000834.5(GRIN2B):c.3799G>A (p.Ala1267Thr) rs141844705
NM_000834.5(GRIN2B):c.3813G>A (p.Ala1271=)
NM_000834.5(GRIN2B):c.3819G>A (p.Thr1273=) rs1555101910
NM_000834.5(GRIN2B):c.465C>T (p.Ser155=) rs115189840
NM_000834.5(GRIN2B):c.618C>T (p.Asp206=)
NM_000834.5(GRIN2B):c.831C>T (p.Leu277=)
NM_000834.5(GRIN2B):c.846T>C (p.Tyr282=) rs1208230861

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