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. 2018 Jun 30;19(7):1931. doi: 10.3390/ijms19071931

Table 1.

Summary of the frequency of recurrent mutations in ENKTL. The overall frequency of mutations is expressed as a percentage of mutated cases out of the total number of cases tested. The reported frequency is available for comparison. Mutations reported in two or more studies are highlighted in bold. See Table S2 for further details.

Gene Reported Frequency No. of Positive Cases (Total No. of Cases Tested) Overall Frequency (%)
ARID1A 6 6 (105) 5.7
ASXL3 4 4 (105) 3.8
BCOR 6–32 20 (147) 13.6
b-catenin 16–30 41 (179) 22.9
BIRC3 3 3 (88) 3.4
BAK 25.9 7 (27) 25.9
CHPF2 4 4 (105) 3.8
C-KIT 5–52 30 (170) 18.8
CMPK1 2 2 (88) 2.3
DDX3X 8–50 33 (283) 11.7
ECSIT 19 17 (88) 19.3
EP300 4–6 7 (156) 4.5
FAT4 2–8 4 (113) 3.5
FAS 4 3 (76) 3.9
IKBKB 2 2 (88) 2.3
IL6R 6 2(34) 5.9
JAK1 2-8 3 (90) 3.3
JAK3 5-35 36 (227) 13
KRAS 3–25 11 (251) 4.4
MLL2 2–18 14(190) 7.4
MLL3 12 3 (25) 12
MSH3 2 2 (88) 2.3
M6PR 2 2 (88) 2.3
MIR17HG 8 2 (25) 8
MSN 9 9 (105) 8.6
MGAM 4 4 (105) 3.8
MGA 9 9 (105) 8.6
NRAS 2–25 6 (227) 2.6
NOTCH2 2–25 3 (153) 2
STAT1 4 1 (25) 4
STAT3 1–26 30 (387) 8.3
STAT5B 2–6 8 (244) 3.3
STAT6 4 1 (25) 4
TP53 4–63 139 (611) 22.7
TET2 8 2 (25) 8
WDR66 2 2 (88) 2.3