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: 99
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HGVS dbSNP
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.411C>A (p.Ile137=) rs146107517
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.6_8CGC[3] (p.Ala6_Ala8del) rs398123566
NM_001110792.2(MECP2):c.6_8CGC[4] (p.Ala7_Ala8del) rs398123566
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.-187_-186delAG rs587783128
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.1029G>C (p.Gly343=) rs1057522816
NM_004992.3(MECP2):c.1041G>A (p.Lys347=) rs1043854626
NM_004992.3(MECP2):c.1060C>T (p.Arg354Cys) rs143876280
NM_004992.3(MECP2):c.1062C>T (p.Arg354=) rs782228941
NM_004992.3(MECP2):c.1071C>T (p.Ser357=) rs61750236
NM_004992.3(MECP2):c.1072G>A (p.Ala358Thr) rs147017239
NM_004992.3(MECP2):c.1075T>C (p.Ser359Pro) rs61752371
NM_004992.3(MECP2):c.1126C>T (p.Pro376Ser) rs61752387
NM_004992.3(MECP2):c.1132G>A (p.Ala378Thr) rs587783106
NM_004992.3(MECP2):c.1132G>T (p.Ala378Ser) rs587783106
NM_004992.3(MECP2):c.1133C>T (p.Ala378Val) rs201314910
NM_004992.3(MECP2):c.1134C>T (p.Ala378=) rs782751264
NM_004992.3(MECP2):c.1138G>A (p.Val380Met) rs267608572
NM_004992.3(MECP2):c.1140G>A (p.Val380=) rs201711454
NM_004992.3(MECP2):c.1147C>T (p.Leu383Phe) rs1340029095
NM_004992.3(MECP2):c.1148_1159del (p.Leu383_Leu386del) rs782767712
NM_004992.3(MECP2):c.1154C>A (p.Pro385His) rs111302745
NM_004992.3(MECP2):c.1160C>T (p.Pro387Leu) rs63390262
NM_004992.3(MECP2):c.1161_1163del (p.Pro391del) rs267608339
NM_004992.3(MECP2):c.1162C>G (p.Pro388Ala) rs61753000
NM_004992.3(MECP2):c.1162_1167CCACCT[1] (p.Pro390_Pro391del) rs61753008
NM_004992.3(MECP2):c.1168C>G (p.Pro390Ala) rs797045690
NM_004992.3(MECP2):c.1171C>G (p.Pro391Ala) rs781794820
NM_004992.3(MECP2):c.1179C>T (p.Pro393=) rs781898011
NM_004992.3(MECP2):c.1180G>A (p.Glu394Lys) rs63094662
NM_004992.3(MECP2):c.1189G>A (p.Glu397Lys) rs56268439
NM_004992.3(MECP2):c.1194C>T (p.Asp398=) rs782741920
NM_004992.3(MECP2):c.1196C>T (p.Pro399Leu) rs62915962
NM_004992.3(MECP2):c.1203C>T (p.Ser401=) rs782230851
NM_004992.3(MECP2):c.1204C>A (p.Pro402Thr) rs150146088
NM_004992.3(MECP2):c.1206C>T (p.Pro402=) rs63586860
NM_004992.3(MECP2):c.1215C>T (p.Pro405=) rs61753964
NM_004992.3(MECP2):c.1234G>A (p.Val412Ile) rs61753966
NM_004992.3(MECP2):c.1237T>C (p.Cys413Arg) rs797045692
NM_004992.3(MECP2):c.1278C>T (p.Ser426=) rs267608619
NM_004992.3(MECP2):c.1282G>A (p.Gly428Ser) rs61753971
NM_004992.3(MECP2):c.1315G>A (p.Ala439Thr) rs61753973
NM_004992.3(MECP2):c.1317G>A (p.Ala439=) rs146632223
NM_004992.3(MECP2):c.1327G>A (p.Ala443Thr) rs193922677
NM_004992.3(MECP2):c.1332C>T (p.Ala444=) rs1204809030
NM_004992.3(MECP2):c.1338C>T (p.Ala446=) rs782496297
NM_004992.3(MECP2):c.1404G>A (p.Arg468=) rs267608633
NM_004992.3(MECP2):c.1412G>C (p.Arg471Thr) rs1057520310
NM_004992.3(MECP2):c.1422T>C (p.Pro474=) rs1557134910
NM_004992.3(MECP2):c.1437G>A (p.Thr479=) rs587781033
NM_004992.3(MECP2):c.225G>A (p.Pro75=) rs61754442
NM_004992.3(MECP2):c.276A>G (p.Gly92=) rs140191561
NM_004992.3(MECP2):c.377+18C>G rs267608461
NM_004992.3(MECP2):c.377+6_377+9delTAAG rs267608459
NM_004992.3(MECP2):c.378-6C>G rs782482746
NM_004992.3(MECP2):c.378T>C (p.Asn126=) rs782035249
NM_004992.3(MECP2):c.381C>G (p.Pro127=) rs782752095
NM_004992.3(MECP2):c.393C>G (p.Ala131=) rs61748385
NM_004992.3(MECP2):c.420G>A (p.Ala140=) rs782082759
NM_004992.3(MECP2):c.516A>G (p.Pro172=) rs1169814545
NM_004992.3(MECP2):c.527C>G (p.Pro176Arg) rs61749701
NM_004992.3(MECP2):c.528C>T (p.Pro176=) rs61754420
NM_004992.3(MECP2):c.54C>A (p.Leu18=) rs372500343
NM_004992.3(MECP2):c.54C>G (p.Leu18=) rs372500343
NM_004992.3(MECP2):c.590C>T (p.Thr197Met) rs61749714
NM_004992.3(MECP2):c.596C>G (p.Pro199Arg) rs267608502
NM_004992.3(MECP2):c.605C>T (p.Ala202Val) rs587783138
NM_004992.3(MECP2):c.633G>C (p.Arg211Ser) rs61749731
NM_004992.3(MECP2):c.660C>T (p.Leu220=) rs267608512
NM_004992.3(MECP2):c.661C>G (p.Leu221Val) rs782357529
NM_004992.3(MECP2):c.686C>T (p.Ser229Leu) rs61749739
NM_004992.3(MECP2):c.717C>A (p.Ala239=) rs1057520963
NM_004992.3(MECP2):c.720C>T (p.Thr240=) rs61749746
NM_004992.3(MECP2):c.727A>G (p.Thr243Ala) rs782145652
NM_004992.3(MECP2):c.750C>A (p.Arg250=) rs61748424
NM_004992.3(MECP2):c.753C>T (p.Pro251=) rs63582063
NM_004992.3(MECP2):c.810A>G (p.Arg270=) rs782743949
NM_004992.3(MECP2):c.815C>T (p.Pro272Leu) rs61750243
NM_004992.3(MECP2):c.841G>A (p.Ala281Thr) rs782239416
NM_004992.3(MECP2):c.849C>G (p.Ala283=) rs61750253
NM_004992.3(MECP2):c.859G>C (p.Ala287Pro) rs61750257
NM_004992.3(MECP2):c.882A>G (p.Arg294=) rs782744332
NM_004992.3(MECP2):c.932C>T (p.Thr311Met) rs61751445
NM_004992.3(MECP2):c.936C>T (p.Val312=) rs398124188
NM_004992.3(MECP2):c.942C>T (p.Ile314=) rs61751446
NM_004992.3(MECP2):c.996C>T (p.Ser332=) rs148744894

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