ClinVar Miner

List of variants in gene MECP2 reported as benign by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Total variants: 32
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HGVS dbSNP
NM_001110792.1(MECP2):c.45_47dupAGG (p.Gly16dup) rs587783744
NM_001110792.2(MECP2):c.1020C>T (p.Leu340=) rs61751442
NM_001110792.2(MECP2):c.1071A>G (p.Lys357=) rs61752362
NM_001110792.2(MECP2):c.1162C>T (p.Pro388Ser) rs61752387
NM_001110792.2(MECP2):c.1169C>T (p.Ala390Val) rs201314910
NM_001110792.2(MECP2):c.1173C>T (p.Pro391=) rs61752980
NM_001110792.2(MECP2):c.1197C>T (p.Pro399=) rs61750246
NM_001110792.2(MECP2):c.1225G>A (p.Glu409Lys) rs56268439
NM_001110792.2(MECP2):c.1233C>T (p.Pro411=) rs61753012
NM_001110792.2(MECP2):c.1269C>T (p.Ser423=) rs3027928
NM_001110792.2(MECP2):c.1270G>A (p.Val424Ile) rs61753966
NM_001110792.2(MECP2):c.1366G>A (p.Ala456Thr) rs61753975
NM_001110792.2(MECP2):c.1371G>A (p.Thr457=) rs3027927
NM_001110792.2(MECP2):c.1409G>A (p.Arg470His) rs185957513
NM_001110792.2(MECP2):c.1473G>A (p.Thr491=) rs587781033
NM_001110792.2(MECP2):c.246C>T (p.Ser82=) rs61754439
NM_001110792.2(MECP2):c.411C>A (p.Ile137=) rs146107517
NM_001110792.2(MECP2):c.462C>T (p.Phe154=) rs61748397
NM_001110792.2(MECP2):c.618C>T (p.Ser206=) rs61749711
NM_001110792.2(MECP2):c.623C>G (p.Thr208Ser) rs61749713
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.644C>T (p.Thr215Met) rs61749720
NM_001110792.2(MECP2):c.719C>G (p.Thr240Ser) rs61749738
NM_001110792.2(MECP2):c.731G>C (p.Gly244Ala) rs61748422
NM_001110792.2(MECP2):c.813C>T (p.Ala271=) rs1042870
NM_001110792.2(MECP2):c.851C>T (p.Pro284Leu) rs61750243
NM_001110792.2(MECP2):c.879C>T (p.Ala293=) rs61750252
NM_001110792.2(MECP2):c.897C>T (p.Ala299=) rs139378224
NM_001110792.2(MECP2):c.933C>T (p.Thr311=) rs61748423
NM_004992.3(MECP2):c.*9G>A rs144008995
NM_004992.3(MECP2):c.378-17del rs61753982

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