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 - databases for immunodeficiency-causing variations

   NHEJ1base
   Variation registry for  Combined immunodeficiency (CID) associated with microcephaly and increased cellular sensitivity to IR


Aminoacid substitutions - NHEJ1base

 - 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 -------55
N ------------0
Q -------------0
S -------0
T -----------0
C ---------1----1
G -----------0
P ------------0
Total 000000000000100000506
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 -------83.383.3
N ------------0.0
Q -------------0.0
S -------0.0
T -----------0.0
C ---------16.7----16.7
G -----------0.0
P ------------0.0
Total 0.00.00.00.00.00.00.00.00.00.00.00.016.70.00.00.00.00.083.30.0100.0