ClinVar Miner

List of variants in gene MECP2 reported as likely benign for Rett syndrome

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Total variants: 13
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NM_001110792.2(MECP2):c.*98dup rs267608341
NM_001110792.2(MECP2):c.1134C>T (p.His378=) rs1557135898
NM_001110792.2(MECP2):c.1174G>A (p.Val392Met) rs267608572
NM_001110792.2(MECP2):c.1198_1203CCACCT[1] (p.Pro402_Pro403del) rs61753008
NM_001110792.2(MECP2):c.1366G>A (p.Ala456Thr) rs61753975
NM_001110792.2(MECP2):c.62+5469A>T rs1557149865
NM_001110792.2(MECP2):c.626C>T (p.Thr209Met) rs61749714
NM_001110792.2(MECP2):c.638C>T (p.Ala213Val) rs61748381
NM_001110792.2(MECP2):c.752C>A (p.Ala251Asp) rs1557136591
NM_001110792.2(MECP2):c.868G>A (p.Ala290Thr) rs782086416
NM_001110792.2(MECP2):c.898G>A (p.Val300Met) rs782455664
NM_004992.3(MECP2):c.378-42A>G rs786205893
NM_004992.3(MECP2):c.378-6C>G rs782482746

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