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 - databases for immunodeficiency-causing variations

   NCF1base
   Variation registry for  Autosomal recessive p47phox deficiency


Aminoacid substitutions - NCF1base

 - 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 -------1------1
H ------------0
K ------------0
R -------33
N ------------0
Q -------------0
S -------0
T -----------0
C -------------0
G ---------10--10
P ------------0
Total 00000000000100310000014
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 -------7.1------7.1
H ------------0.0
K ------------0.0
R -------21.421.4
N ------------0.0
Q -------------0.0
S -------0.0
T -----------0.0
C -------------0.0
G ---------71.4--71.4
P ------------0.0
Total 0.00.00.00.00.00.00.00.00.00.00.07.10.00.021.471.40.00.00.00.0100.0