Skip to main content
. Author manuscript; available in PMC: 2016 Jul 1.
Published in final edited form as: Ann Hematol. 2015 Mar 7;94(7):1205–1211. doi: 10.1007/s00277-015-2344-9

Table 2.

This table illustrates the individual change of the mutational profile over time tracked by M3P

TP 1 TP 2
FAM46C 87 % 83 %
KRAS 57 % 51 %
SP140 81 % 22 %
TP53 78 % 90 %
82 % 0 %
0 % 84 %

Percentage in box represents purity corrected variant reads. In this patient one TP53 mutation gets eradicated over time, whereas a second TP53 mutation expands between the time points, suggesting the presence of at least two different clones. Additionally, a SP140 mutation is decreased but not eradicated, suggesting the existence of a third clone. Furthermore, the mutation frequency of a FAM46C, a KRAS and a third TP53 mutation stay unchanged over time and are not affected by the clonal evolution tracked by M3 P, providing evidence that these mutations are clonal