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 - databases for immunodeficiency-causing variations

   NCF2base
   Variation registry for  Autosomal recessive p67phox deficiency


Aminoacid substitutions - NCF2base

 - indicates amino acid change that require more complex mutation than single nucleotide substitution.
Aminoacid substitutions
Hydrophilic
HydrophobicAcidicBasicPolarSpecial
--> AFILMVWYDEHKRNQSTCGPTotal
A ----13--------13
F -------------0
I ----------0
L ---------0
M ---1-----------1
V -----------0
W -----------2----2
Y -------------0
D ----3-14-------17
E -------------0
H ------------0
K -------1-2----3
R ---4----3310
N --2-------2---4
Q --------2-----2
S -------0
T -----------0
C -------------0
G -----2--4---2-8
P ------------0
Total 002001740019026032020360
Aminoacid substitutions (%)
Hydrophilic
HydrophobicAcidicBasicPolarSpecial
--> AFILMVWYDEHKRNQSTCGPTotal
A ----21.7--------21.7
F -------------0.0
I ----------0.0
L ---------0.0
M ---1.7-----------1.7
V -----------0.0
W -----------3.3----3.3
Y -------------0.0
D ----5.0-23.3-------28.3
E -------------0.0
H ------------0.0
K -------1.7-3.3----5.0
R ---6.7----5.05.016.7
N --3.3-------3.3---6.7
Q --------3.3-----3.3
S -------0.0
T -----------0.0
C -------------0.0
G -----3.3--6.7---3.3-13.3
P ------------0.0
Total 0.00.03.30.00.028.36.70.00.031.70.03.310.00.05.03.30.03.30.05.0100.0