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- databases for immunodeficiency-causing variations

   NCF1base
   Variation registry for  Autosomal recessive p47phox deficiency


Nucleotide substitutions - NCF1base

Purines/Pyrimidines
PurinesPyrimidines
-->AGCTTotal
A 0 0 0 0 0
G 60 0 2 1 63
C 0 0 0 3 3
T 3 2 0 0 5
Total 63 2 2 4 71
Amino/Keto
AminoKeto
-->ACGTTotal
A 0 0 0 0 0
C 0 0 0 3 3
G 60 2 0 1 63
T 3 0 2 0 5
Total 63 2 2 4 71
Weak/Strong
WeakStrong
-->ATCGTotal
A 0 0 0 0 0
T 3 0 0 2 5
C 0 3 0 0 3
G 60 1 2 0 63
Total 63 4 2 2 71
Purines/Pyrimidines (%)
PurinesPyrimidines
-->AGCTTotal
A 0.0 0.0 0.0 0.0 0.0
G 84.5 0.0 2.8 1.4 88.7
C 0.0 0.0 0.0 4.2 4.2
T 4.2 2.8 0.0 0.0 7.0
Total 88.7 2.8 2.8 5.6 100.0
Amino/Keto (%)
AminoKeto
-->ACGTTotal
A 0.0 0.0 0.0 0.0 0.0
C 0.0 0.0 0.0 4.2 4.2
G 84.5 2.8 0.0 1.4 88.7
T 4.2 0.0 2.8 0.0 7.0
Total 88.7 2.8 2.8 5.6 100.0
Weak/Strong (%)
WeakStrong
-->ATCGTotal
A 0.0 0.0 0.0 0.0 0.0
T 4.2 0.0 0.0 2.8 7.0
C 0.0 4.2 0.0 0.0 4.2
G 84.5 1.4 2.8 0.0 88.7
Total 88.7 5.6 2.8 2.8 100.0
Transitions and Transversions
-->PurinePyrimidine
Purine603
Pyrimidine53

Transitions and Transversions (%)
-->PurinePyrimidine
Purine84.54.2
Pyrimidine7.04.2