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- databases for immunodeficiency-causing variations

   NCF2base
   Variation registry for  Autosomal recessive p67phox deficiency


Nucleotide substitutions - NCF2base

Purines/Pyrimidines
PurinesPyrimidines
-->AGCTTotal
A 0 4 0 9 13
G 28 0 17 5 50
C 0 16 0 61 77
T 2 0 4 0 6
Total 30 20 21 75 146
Amino/Keto
AminoKeto
-->ACGTTotal
A 0 0 4 9 13
C 0 0 16 61 77
G 28 17 0 5 50
T 2 4 0 0 6
Total 30 21 20 75 146
Weak/Strong
WeakStrong
-->ATCGTotal
A 0 9 0 4 13
T 2 0 4 0 6
C 0 61 0 16 77
G 28 5 17 0 50
Total 30 75 21 20 146
Purines/Pyrimidines (%)
PurinesPyrimidines
-->AGCTTotal
A 0.0 2.7 0.0 6.2 8.9
G 19.2 0.0 11.6 3.4 34.2
C 0.0 11.0 0.0 41.8 52.7
T 1.4 0.0 2.7 0.0 4.1
Total 20.5 13.7 14.4 51.4 100.0
Amino/Keto (%)
AminoKeto
-->ACGTTotal
A 0.0 0.0 2.7 6.2 8.9
C 0.0 0.0 11.0 41.8 52.7
G 19.2 11.6 0.0 3.4 34.2
T 1.4 2.7 0.0 0.0 4.1
Total 20.5 14.4 13.7 51.4 100.0
Weak/Strong (%)
WeakStrong
-->ATCGTotal
A 0.0 6.2 0.0 2.7 8.9
T 1.4 0.0 2.7 0.0 4.1
C 0.0 41.8 0.0 11.0 52.7
G 19.2 3.4 11.6 0.0 34.2
Total 20.5 51.4 14.4 13.7 100.0
Transitions and Transversions
-->PurinePyrimidine
Purine3231
Pyrimidine1865

Transitions and Transversions (%)
-->PurinePyrimidine
Purine21.921.2
Pyrimidine12.344.5