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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


Nucleotide substitutions - NHEJ1base

Purines/Pyrimidines
PurinesPyrimidines
-->AGCTTotal
A 0 0 0 4 4
G 0 0 0 0 0
C 0 5 0 5 10
T 0 0 1 0 1
Total 0 5 1 9 15
Amino/Keto
AminoKeto
-->ACGTTotal
A 0 0 0 4 4
C 0 0 5 5 10
G 0 0 0 0 0
T 0 1 0 0 1
Total 0 1 5 9 15
Weak/Strong
WeakStrong
-->ATCGTotal
A 0 4 0 0 4
T 0 0 1 0 1
C 0 5 0 5 10
G 0 0 0 0 0
Total 0 9 1 5 15
Purines/Pyrimidines (%)
PurinesPyrimidines
-->AGCTTotal
A 0.0 0.0 0.0 26.7 26.7
G 0.0 0.0 0.0 0.0 0.0
C 0.0 33.3 0.0 33.3 66.7
T 0.0 0.0 6.7 0.0 6.7
Total 0.0 33.3 6.7 60.0 100.0
Amino/Keto (%)
AminoKeto
-->ACGTTotal
A 0.0 0.0 0.0 26.7 26.7
C 0.0 0.0 33.3 33.3 66.7
G 0.0 0.0 0.0 0.0 0.0
T 0.0 6.7 0.0 0.0 6.7
Total 0.0 6.7 33.3 60.0 100.0
Weak/Strong (%)
WeakStrong
-->ATCGTotal
A 0.0 26.7 0.0 0.0 26.7
T 0.0 0.0 6.7 0.0 6.7
C 0.0 33.3 0.0 33.3 66.7
G 0.0 0.0 0.0 0.0 0.0
Total 0.0 60.0 6.7 33.3 100.0
Transitions and Transversions
-->PurinePyrimidine
Purine04
Pyrimidine56

Transitions and Transversions (%)
-->PurinePyrimidine
Purine0.026.7
Pyrimidine33.340.0