Table 3.

Mutation patterns of the PAX5, RhoH/TTF, c-MYC, and PIM1 genes


Gene

All mutations

del/ins

A

T

G

C

TS

TV

RGYW WRCY
PAX5 (%)   65 (100)   3 (5)   3 (5)   1 (2)   35 (53)   23 (35)   39 (60)   23 (35)   22 (34)  
RhoH/TTF (%)   25 (100)   0 (0)   0 (0)   4 (16)   14 (56)   7 (28)   16 (64)   9 (36)   14 (56)  
c-MYC (%)   16 (100)   0 (0)   0 (0)   1 (6)   7 (44)   8 (50)   8 (50)   8 (50)   4 (25)  
PIM1 (%)   19 (100)   0 (0)   1 (5)   1 (5)   9 (47)   8 (43)   9 (47)   10 (53)   7 (37)  
Σ (%)
 
125 (100)
 
3 (2)
 
4 (3)
 
7 (6)
 
65 (52)
 
46 (37)
 
72 (58)
 
50 (40)
 
47 (38)
 

Gene

All mutations

del/ins

A

T

G

C

TS

TV

RGYW WRCY
PAX5 (%)   65 (100)   3 (5)   3 (5)   1 (2)   35 (53)   23 (35)   39 (60)   23 (35)   22 (34)  
RhoH/TTF (%)   25 (100)   0 (0)   0 (0)   4 (16)   14 (56)   7 (28)   16 (64)   9 (36)   14 (56)  
c-MYC (%)   16 (100)   0 (0)   0 (0)   1 (6)   7 (44)   8 (50)   8 (50)   8 (50)   4 (25)  
PIM1 (%)   19 (100)   0 (0)   1 (5)   1 (5)   9 (47)   8 (43)   9 (47)   10 (53)   7 (37)  
Σ (%)
 
125 (100)
 
3 (2)
 
4 (3)
 
7 (6)
 
65 (52)
 
46 (37)
 
72 (58)
 
50 (40)
 
47 (38)
 

del/ins indicates number of deletions and insertions; A, mutations occurring at adenosine position; T, analogous to A; G, analogous to A; C, analogous to A; RGYW/WRCY, number of mutations embedded in the mutational hot spot motive RGYW (R = A, G; Y = C, T; W = A, T); TS, transitions; TV, transversions; and Σ, the sum of the mutations in the respective column.

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