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. 2012 Aug 6;13:68. doi: 10.1186/1471-2350-13-68

Table 1.

CDKL5 mutation/variant identified in this study

Total number of females studied* Number of DNA variants* Location Nucleotide change Aminoacid change Domain Effect Reference**
60 p
1 p
Exon 8
c.509_510insGT
p.Glu170GlyfsX36
Catalytic
Pathogenic
NEW, this study
60 p
1 p
Exon 10
c.745-?_825 + ?del
----------
Catalytic
Pathogenic
NEW, this study
160 (60p + 100c)
1 p
Exon 12
c.1455_1460delGGCCAA
p.Ala486_Lys487del
C-Ter
Unknown Variation
NEW, this study
160 (60p + 100c)
7 (1p + 6 c)
Exon 17
c.2389 G > A
p.Asp797Asn
C-Ter
Polymorphism
NEW, this study
160 (60p + 100c)
6 (1p + 5 c)
Before exon 1
c.-426 C > G
----------
------
Polymorphism
NEW, this study
60 p
1 p
Intron 6
c.403 + 27A > G
----------
------
Without pathogenic effect
NEW, this study
160 (60p + 100c)
2 (1p + 1c)
Exon 21
c.2995 G > A
p.Val999Met
C-Ter
Polymorphism (SNP: rs35693326)
Nectoux et al. [26] Intusoma et al. [27]
160 (60p + 100c)
6 (2p + 4c)
Before exon 1
c.-391 G > T
----------
------
Polymorphism
Evans et al. [12]
60 p 2 p Exon 4, 21 c.145 + 17A > G; c. 3003 C > G; c. 3084 G > A p.His1001His; p.Thr1028Thr Catalytic, C-Ter Polymorphism Tao et al. [28]

*p: Female patients; c: control healthy females.

** New mutations/variants have not been described in any of the 10 Genome databases revised [15-24].

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