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 - databases for immunodeficiency-causing variations

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


Aminoacid substitutions - NFKBIAbase

 - indicates amino acid change that require more complex mutation than single nucleotide substitution.
Aminoacid substitutions
Hydrophilic
HydrophobicAcidicBasicPolarSpecial
--> AFILMVWYDEHKRNQSTCGPTotal
A ------------0
F -------------0
I ----------0
L ---------0
M --------------0
V -----------0
W ---------------0
Y -------------0
D ------------0
E -------------0
H ------------0
K ------------0
R -------0
N ------------0
Q -------------0
S 1-------1
T -----------0
C -------------0
G -----------0
P ------------0
Total 001000000000000000001
Aminoacid substitutions (%)
Hydrophilic
HydrophobicAcidicBasicPolarSpecial
--> AFILMVWYDEHKRNQSTCGPTotal
A ------------0.0
F -------------0.0
I ----------0.0
L ---------0.0
M --------------0.0
V -----------0.0
W ---------------0.0
Y -------------0.0
D ------------0.0
E -------------0.0
H ------------0.0
K ------------0.0
R -------0.0
N ------------0.0
Q -------------0.0
S 100.0-------100.0
T -----------0.0
C -------------0.0
G -----------0.0
P ------------0.0
Total 0.00.0100.00.00.00.00.00.00.00.00.00.00.00.00.00.00.00.00.00.0100.0