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 - databases for immunodeficiency-causing variations

   HAX1base
   Variation registry for  Severe congenital neutropenia (Kostmann disease)


Aminoacid substitutions - HAX1base

 - indicates amino acid change that require more complex mutation than single nucleotide substitution.
Aminoacid substitutions
Hydrophilic
HydrophobicAcidicBasicPolarSpecial
--> AFILMVWYDEHKRNQSTCGPTotal
A ------------0
F -4------------4
I ----------0
L -----2----2
M --------------0
V 1----------3-4
W ---------------0
Y -------------0
D ------------0
E -------------0
H ------------0
K ------------0
R -------0
N ------------0
Q -------------0
S -------0
T -----------0
C -------------0
G -----------0
P ------------0
Total 0014000000002000003010
Aminoacid substitutions (%)
Hydrophilic
HydrophobicAcidicBasicPolarSpecial
--> AFILMVWYDEHKRNQSTCGPTotal
A ------------0.0
F -40.0------------40.0
I ----------0.0
L -----20.0----20.0
M --------------0.0
V 10.0----------30.0-40.0
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 -------0.0
T -----------0.0
C -------------0.0
G -----------0.0
P ------------0.0
Total 0.00.010.040.00.00.00.00.00.00.00.00.020.00.00.00.00.00.030.00.0100.0