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- databases for immunodeficiency-causing variations

   NFKBIAbase
   Variation registry for  Autosomal dominant anhidrotic ectodermal dysplasia and T-cell immunodeficiency


Nucleotide substitutions - NFKBIAbase

Purines/Pyrimidines
PurinesPyrimidines
-->AGCTTotal
A 0 0 0 0 0
G 0 0 0 2 2
C 0 0 0 0 0
T 0 0 0 0 0
Total 0 0 0 2 2
Amino/Keto
AminoKeto
-->ACGTTotal
A 0 0 0 0 0
C 0 0 0 0 0
G 0 0 0 2 2
T 0 0 0 0 0
Total 0 0 0 2 2
Weak/Strong
WeakStrong
-->ATCGTotal
A 0 0 0 0 0
T 0 0 0 0 0
C 0 0 0 0 0
G 0 2 0 0 2
Total 0 2 0 0 2
Purines/Pyrimidines (%)
PurinesPyrimidines
-->AGCTTotal
A 0.0 0.0 0.0 0.0 0.0
G 0.0 0.0 0.0 100.0 100.0
C 0.0 0.0 0.0 0.0 0.0
T 0.0 0.0 0.0 0.0 0.0
Total 0.0 0.0 0.0 100.0 100.0
Amino/Keto (%)
AminoKeto
-->ACGTTotal
A 0.0 0.0 0.0 0.0 0.0
C 0.0 0.0 0.0 0.0 0.0
G 0.0 0.0 0.0 100.0 100.0
T 0.0 0.0 0.0 0.0 0.0
Total 0.0 0.0 0.0 100.0 100.0
Weak/Strong (%)
WeakStrong
-->ATCGTotal
A 0.0 0.0 0.0 0.0 0.0
T 0.0 0.0 0.0 0.0 0.0
C 0.0 0.0 0.0 0.0 0.0
G 0.0 100.0 0.0 0.0 100.0
Total 0.0 100.0 0.0 0.0 100.0
Transitions and Transversions
-->PurinePyrimidine
Purine02
Pyrimidine00

Transitions and Transversions (%)
-->PurinePyrimidine
Purine0.0100.0
Pyrimidine0.00.0