NM_001110792.2(MECP2):c.414-61C>G
|
rs191076920
|
0.00056
|
NM_001110792.2(MECP2):c.1174G>A (p.Val392Met)
|
rs267608572
|
0.00022
|
NM_001110792.2(MECP2):c.1196C>T (p.Pro399Leu)
|
rs63390262
|
0.00010
|
NM_001110792.2(MECP2):c.1363G>A (p.Ala455Thr)
|
rs193922677
|
0.00009
|
NM_001110792.2(MECP2):c.1469G>A (p.Arg490Gln)
|
rs145790362
|
0.00005
|
NM_001110792.2(MECP2):c.1250C>T (p.Pro417Leu)
|
rs61753016
|
0.00004
|
NM_001110792.2(MECP2):c.838C>T (p.Arg280Trp)
|
rs61750239
|
0.00004
|
NM_001110792.2(MECP2):c.1291C>T (p.Pro431Ser)
|
rs140258520
|
0.00003
|
NM_001110792.2(MECP2):c.968C>T (p.Thr323Met)
|
rs61751445
|
0.00003
|
NM_001110792.2(MECP2):c.1049C>G (p.Thr350Ser)
|
rs786204313
|
0.00002
|
NM_001110792.2(MECP2):c.1187C>T (p.Pro396Leu)
|
rs193922676
|
0.00002
|
NM_001110792.2(MECP2):c.553C>G (p.Pro185Ala)
|
rs61748427
|
0.00002
|
NM_001110792.2(MECP2):c.727G>A (p.Gly243Arg)
|
rs587783139
|
0.00002
|
NM_001110792.2(MECP2):c.1394G>A (p.Arg465Gln)
|
rs61753980
|
0.00001
|
NM_001110792.2(MECP2):c.413+24C>A
|
rs267608462
|
0.00001
|
NM_001110792.1(MECP2):c.-46_-45delGC
|
rs782107551
|
|
NM_001110792.2(MECP2):c.-27_-26delinsTT
|
rs786205039
|
|
NM_001110792.2(MECP2):c.-31AG[2]
|
rs587783128
|
|
NM_001110792.2(MECP2):c.1130A>G (p.Glu377Gly)
|
|
|
NM_001110792.2(MECP2):c.1147C>T (p.His383Tyr)
|
rs2148661028
|
|
NM_001110792.2(MECP2):c.1197_1436del (p.Pro400_Pro479del)
|
rs1557134946
|
|
NM_001110792.2(MECP2):c.1269_1279del (p.Ser423fs)
|
rs786205036
|
|
NM_001110792.2(MECP2):c.49G>A (p.Glu17Lys)
|
rs786205046
|
|
NM_001110792.2(MECP2):c.515C>A (p.Thr172Asn)
|
|
|
NM_001110792.2(MECP2):c.535C>T (p.Arg179Trp)
|
rs61748420
|
|
NM_001110792.2(MECP2):c.550C>T (p.Pro184Ser)
|
rs61748426
|
|
NM_001110792.2(MECP2):c.580C>T (p.Pro194Ser)
|
|
|
NM_001110792.2(MECP2):c.6CGC[4] (p.Ala7_Ala8del)
|
rs398123566
|
|
NM_001110792.2(MECP2):c.6CGC[9] (p.Ala6_Ala8dup)
|
rs398123566
|
|
NM_001110792.2(MECP2):c.715C>G (p.Gln239Glu)
|
rs61749737
|
|
NM_001110792.2(MECP2):c.724C>A (p.Pro242Thr)
|
rs1209806388
|
|
NM_001110792.2(MECP2):c.818C>G (p.Pro273Arg)
|
|
|
NM_001110792.2(MECP2):c.872C>T (p.Ala291Val)
|
rs61750249
|
|
NM_001110792.2(MECP2):c.886A>G (p.Lys296Glu)
|
rs61750255
|
|
NM_001110792.2(MECP2):c.945C>G (p.Ile315Met)
|
rs61751439
|
|
NM_001110792.2(MECP2):c.961C>T (p.Arg321Trp)
|
rs61751444
|
|
NM_001110792.2(MECP2):c.991G>A (p.Val331Met)
|
rs1569548388
|
|
NM_004992.3:c.(?_-226)_(*1_?)dup
|
|
|