ClinVar Miner

List of variants in gene MECP2 reported as likely benign for not specified

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Gene type:
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Total variants: 101
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HGVS dbSNP
NM_001110792.2(MECP2):c.-31_-30AG[2] rs587783128
NM_001110792.2(MECP2):c.1017C>T (p.Thr339=) rs1015722593
NM_001110792.2(MECP2):c.1032C>T (p.Ser344=) rs148744894
NM_001110792.2(MECP2):c.1065G>C (p.Gly355=) rs1057522816
NM_001110792.2(MECP2):c.1077G>A (p.Lys359=) rs1043854626
NM_001110792.2(MECP2):c.1096C>T (p.Arg366Cys) rs143876280
NM_001110792.2(MECP2):c.1098C>T (p.Arg366=) rs782228941
NM_001110792.2(MECP2):c.1107C>T (p.Ser369=) rs61750236
NM_001110792.2(MECP2):c.1108G>A (p.Ala370Thr) rs147017239
NM_001110792.2(MECP2):c.1111T>C (p.Ser371Pro) rs61752371
NM_001110792.2(MECP2):c.1162C>T (p.Pro388Ser) rs61752387
NM_001110792.2(MECP2):c.1168G>A (p.Ala390Thr) rs587783106
NM_001110792.2(MECP2):c.1168G>T (p.Ala390Ser) rs587783106
NM_001110792.2(MECP2):c.1169C>T (p.Ala390Val) rs201314910
NM_001110792.2(MECP2):c.1170C>T (p.Ala390=) rs782751264
NM_001110792.2(MECP2):c.1174G>A (p.Val392Met) rs267608572
NM_001110792.2(MECP2):c.1176G>A (p.Val392=) rs201711454
NM_001110792.2(MECP2):c.1183C>T (p.Leu395Phe) rs1340029095
NM_001110792.2(MECP2):c.1184_1195del (p.Leu395_Leu398del) rs782767712
NM_001110792.2(MECP2):c.1190C>A (p.Pro397His) rs111302745
NM_001110792.2(MECP2):c.1196C>T (p.Pro399Leu) rs63390262
NM_001110792.2(MECP2):c.1197_1199del (p.Pro403del) rs267608339
NM_001110792.2(MECP2):c.1198C>G (p.Pro400Ala) rs61753000
NM_001110792.2(MECP2):c.1198_1203CCACCT[1] (p.Pro402_Pro403del) rs61753008
NM_001110792.2(MECP2):c.1204C>G (p.Pro402Ala) rs797045690
NM_001110792.2(MECP2):c.1207C>G (p.Pro403Ala) rs781794820
NM_001110792.2(MECP2):c.1215C>T (p.Pro405=) rs781898011
NM_001110792.2(MECP2):c.1216G>A (p.Glu406Lys) rs63094662
NM_001110792.2(MECP2):c.1225G>A (p.Glu409Lys) rs56268439
NM_001110792.2(MECP2):c.1230C>T (p.Asp410=) rs782741920
NM_001110792.2(MECP2):c.1232C>T (p.Pro411Leu) rs62915962
NM_001110792.2(MECP2):c.1239C>T (p.Ser413=) rs782230851
NM_001110792.2(MECP2):c.1240C>A (p.Pro414Thr) rs150146088
NM_001110792.2(MECP2):c.1242C>T (p.Pro414=) rs63586860
NM_001110792.2(MECP2):c.1251C>T (p.Pro417=) rs61753964
NM_001110792.2(MECP2):c.1270G>A (p.Val424Ile) rs61753966
NM_001110792.2(MECP2):c.1273T>C (p.Cys425Arg) rs797045692
NM_001110792.2(MECP2):c.1314C>T (p.Ser438=) rs267608619
NM_001110792.2(MECP2):c.1318G>A (p.Gly440Ser) rs61753971
NM_001110792.2(MECP2):c.1351G>A (p.Ala451Thr) rs61753973
NM_001110792.2(MECP2):c.1353G>A (p.Ala451=) rs146632223
NM_001110792.2(MECP2):c.1363G>A (p.Ala455Thr) rs193922677
NM_001110792.2(MECP2):c.1368C>T (p.Ala456=) rs1204809030
NM_001110792.2(MECP2):c.1374C>T (p.Ala458=) rs782496297
NM_001110792.2(MECP2):c.1440G>A (p.Arg480=) rs267608633
NM_001110792.2(MECP2):c.1448G>C (p.Arg483Thr) rs1057520310
NM_001110792.2(MECP2):c.1458T>C (p.Pro486=) rs1557134910
NM_001110792.2(MECP2):c.1473G>A (p.Thr491=) rs587781033
NM_001110792.2(MECP2):c.261G>A (p.Pro87=) rs61754442
NM_001110792.2(MECP2):c.312A>G (p.Gly104=) rs140191561
NM_001110792.2(MECP2):c.33_35AGG[4] (p.Gly16del) rs587783744
NM_001110792.2(MECP2):c.33_35AGG[7] (p.Gly15_Gly16dup) rs587783744
NM_001110792.2(MECP2):c.414T>C (p.Asn138=) rs782035249
NM_001110792.2(MECP2):c.417C>G (p.Pro139=) rs782752095
NM_001110792.2(MECP2):c.429C>G (p.Ala143=) rs61748385
NM_001110792.2(MECP2):c.44G>A (p.Gly15Glu) rs1333935838
NM_001110792.2(MECP2):c.44_49dup (p.Gly15_Gly16dup) rs1064795312
NM_001110792.2(MECP2):c.456G>A (p.Ala152=) rs782082759
NM_001110792.2(MECP2):c.528C>T (p.Ser176=) rs1557136964
NM_001110792.2(MECP2):c.550C>A (p.Pro184Thr)
NM_001110792.2(MECP2):c.552A>G (p.Pro184=) rs1169814545
NM_001110792.2(MECP2):c.563C>G (p.Pro188Arg) rs61749701
NM_001110792.2(MECP2):c.564C>T (p.Pro188=) rs61754420
NM_001110792.2(MECP2):c.626C>T (p.Thr209Met) rs61749714
NM_001110792.2(MECP2):c.632C>G (p.Pro211Arg) rs267608502
NM_001110792.2(MECP2):c.641C>T (p.Ala214Val) rs587783138
NM_001110792.2(MECP2):c.669G>C (p.Arg223Ser) rs61749731
NM_001110792.2(MECP2):c.696C>T (p.Leu232=) rs267608512
NM_001110792.2(MECP2):c.697C>G (p.Leu233Val) rs782357529
NM_001110792.2(MECP2):c.6_8CGC[3] (p.Ala6_Ala8del) rs398123566
NM_001110792.2(MECP2):c.6_8CGC[4] (p.Ala7_Ala8del) rs398123566
NM_001110792.2(MECP2):c.722C>T (p.Ser241Leu) rs61749739
NM_001110792.2(MECP2):c.753C>A (p.Ala251=) rs1057520963
NM_001110792.2(MECP2):c.756C>T (p.Thr252=) rs61749746
NM_001110792.2(MECP2):c.763A>G (p.Thr255Ala) rs782145652
NM_001110792.2(MECP2):c.786C>A (p.Arg262=) rs61748424
NM_001110792.2(MECP2):c.789C>T (p.Pro263=) rs63582063
NM_001110792.2(MECP2):c.846A>G (p.Arg282=) rs782743949
NM_001110792.2(MECP2):c.851C>T (p.Pro284Leu) rs61750243
NM_001110792.2(MECP2):c.877G>A (p.Ala293Thr) rs782239416
NM_001110792.2(MECP2):c.885C>G (p.Ala295=) rs61750253
NM_001110792.2(MECP2):c.895G>C (p.Ala299Pro) rs61750257
NM_001110792.2(MECP2):c.90C>A (p.Leu30=) rs372500343
NM_001110792.2(MECP2):c.90C>G (p.Leu30=) rs372500343
NM_001110792.2(MECP2):c.918A>G (p.Arg306=) rs782744332
NM_001110792.2(MECP2):c.968C>T (p.Thr323Met) rs61751445
NM_001110792.2(MECP2):c.972C>T (p.Val324=) rs398124188
NM_001110792.2(MECP2):c.978C>T (p.Ile326=) rs61751446
NM_004992.3(MECP2):c.*13C>T rs782334844
NM_004992.3(MECP2):c.*14G>A rs199963992
NM_004992.3(MECP2):c.*16A>G rs1057520854
NM_004992.3(MECP2):c.*1C>G rs781782964
NM_004992.3(MECP2):c.-174A>C rs1557150926
NM_004992.3(MECP2):c.-195T>G rs1335569199
NM_004992.3(MECP2):c.-203C>G rs1057524091
NM_004992.3(MECP2):c.-95C>G rs782519280
NM_004992.3(MECP2):c.-99+20C>A rs781969166
NM_004992.3(MECP2):c.-99+20C>G rs781969166
NM_004992.3(MECP2):c.377+18C>G rs267608461
NM_004992.3(MECP2):c.377+6_377+9del rs267608459
NM_004992.3(MECP2):c.378-6C>G rs782482746

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