ClinVar Miner

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

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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_001110792.2(MECP2):c.1225G>A (p.Glu409Lys) rs56268439 0.00308
NM_001110792.2(MECP2):c.626C>T (p.Thr209Met) rs61749714 0.00064
NM_001110792.2(MECP2):c.885C>G (p.Ala295=) rs61750253 0.00042
NM_001110792.2(MECP2):c.*14G>A rs199963992 0.00037
NM_001110792.2(MECP2):c.978C>T (p.Ile326=) rs61751446 0.00034
NM_001110792.2(MECP2):c.429C>G (p.Ala143=) rs61748385 0.00018
NM_001110792.2(MECP2):c.1176G>A (p.Val392=) rs201711454 0.00015
NM_001110792.2(MECP2):c.*13C>T rs782334844 0.00013
NM_001110792.2(MECP2):c.789C>T (p.Pro263=) rs63582063 0.00013
NM_001110792.2(MECP2):c.1032C>T (p.Ser344=) rs148744894 0.00012
NM_001110792.2(MECP2):c.669G>C (p.Arg223Ser) rs61749731 0.00012
NM_001110792.2(MECP2):c.1196C>T (p.Pro399Leu) rs63390262 0.00010
NM_001110792.2(MECP2):c.1216G>A (p.Glu406Lys) rs63094662 0.00009
NM_001110792.2(MECP2):c.756C>T (p.Thr252=) rs61749746 0.00009
NM_001110792.2(MECP2):c.1096C>T (p.Arg366Cys) rs143876280 0.00007
NM_001110792.2(MECP2):c.1107C>T (p.Ser369=) rs61750236 0.00006
NM_001110792.2(MECP2):c.1111T>C (p.Ser371Pro) rs61752371 0.00005
NM_001110792.2(MECP2):c.456G>A (p.Ala152=) rs782082759 0.00005
NM_001110792.2(MECP2):c.563C>G (p.Pro188Arg) rs61749701 0.00005
NM_001110792.2(MECP2):c.696C>T (p.Leu232=) rs267608512 0.00005
NM_001110792.2(MECP2):c.1190C>A (p.Pro397His) rs111302745 0.00004
NM_001110792.2(MECP2):c.877G>A (p.Ala293Thr) rs782239416 0.00004
NM_001110792.2(MECP2):c.1314C>T (p.Ser438=) rs267608619 0.00003
NM_001110792.2(MECP2):c.1374C>T (p.Ala458=) rs782496297 0.00003
NM_001110792.2(MECP2):c.261G>A (p.Pro87=) rs61754442 0.00003
NM_001110792.2(MECP2):c.417C>G (p.Pro139=) rs782752095 0.00003
NM_001110792.2(MECP2):c.968C>T (p.Thr323Met) rs61751445 0.00003
NM_001110792.2(MECP2):c.1168G>A (p.Ala390Thr) rs587783106 0.00002
NM_001110792.2(MECP2):c.413+18C>G rs267608461 0.00002
NM_001110792.2(MECP2):c.414T>C (p.Asn138=) rs782035249 0.00002
NM_001110792.2(MECP2):c.62+20C>G rs781969166 0.00002
NM_001110792.2(MECP2):c.632C>G (p.Pro211Arg) rs267608502 0.00002
NM_001110792.2(MECP2):c.895G>C (p.Ala299Pro) rs61750257 0.00002
NM_001110792.2(MECP2):c.*16A>G rs1057520854 0.00001
NM_001110792.2(MECP2):c.1017C>T (p.Thr339=) rs1015722593 0.00001
NM_001110792.2(MECP2):c.1170C>T (p.Ala390=) rs782751264 0.00001
NM_001110792.2(MECP2):c.1183C>T (p.Leu395Phe) rs1340029095 0.00001
NM_001110792.2(MECP2):c.1368C>T (p.Ala456=) rs1204809030 0.00001
NM_001110792.2(MECP2):c.44G>A (p.Gly15Glu) rs1333935838 0.00001
NM_001110792.2(MECP2):c.552A>G (p.Pro184=) rs1169814545 0.00001
NM_001110792.2(MECP2):c.62+5300C>G rs782519280 0.00001
NM_001110792.2(MECP2):c.763A>G (p.Thr255Ala) rs782145652 0.00001
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.1169C>T (p.Ala390Val) rs201314910
NM_001110792.2(MECP2):c.1184_1195del (p.Leu395_Leu398del) rs782767712
NM_001110792.2(MECP2):c.1197_1199del (p.Pro403del) rs267608339
NM_001110792.2(MECP2):c.1198CCACCT[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.1273T>C (p.Cys425Arg) rs797045692
NM_001110792.2(MECP2):c.1351G>A (p.Ala451Thr) rs61753973
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.33AGG[6] (p.Gly16dup) rs587783744
NM_001110792.2(MECP2):c.413+6_413+9del rs267608459
NM_001110792.2(MECP2):c.528C>T (p.Ser176=) rs1557136964
NM_001110792.2(MECP2):c.550C>A (p.Pro184Thr) rs61748426
NM_001110792.2(MECP2):c.564C>T (p.Pro188=) rs61754420
NM_001110792.2(MECP2):c.62+20C>A rs781969166
NM_001110792.2(MECP2):c.641C>T (p.Ala214Val) rs587783138
NM_001110792.2(MECP2):c.697C>G (p.Leu233Val) rs782357529
NM_001110792.2(MECP2):c.753C>A (p.Ala251=) rs1057520963
NM_001110792.2(MECP2):c.786C>G (p.Arg262=) rs61748424
NM_001110792.2(MECP2):c.90C>A (p.Leu30=) rs372500343
NM_001110792.2(MECP2):c.972C>T (p.Val324=) rs398124188

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