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. 2020 Oct 14;10(10):101. doi: 10.1038/s41408-020-00367-2

Table 2.

Summary of relapse-specific coding driver mutations, promoter mutations, CRE mutations, driver translocations, and large-scale genomic changes identified in 24 primary tumour-relapse pairs grouped by subtype.

Subtype Coding drivers Promoters CREs Driver translocations Frequent large-scale genomic changes
t(4;14) KRAS; TP53; FGFR3; FAM46C; TRAF2; NF1; XBP1 MTFRL1; FLT3LG; IL12A; POLG; XBP1; B3GALNT1; ALG10B ABCA10; ABCA5 MAP3K14 t(17,14)(q21,q32)

17p deletion

Further copy number changes at unstable genomic regions (11q and 14q)

Increased telomere length

t(11;14) PRDM1; LTB; IDH2; KRAS; NRAS; CCND1; ATM; FAM154B; MLL3 RBX1; FAM81A; POLG; KCTD13; SCML1 SCAF8
t(14;16) NRAS; TET2 MYO1E; ALG10B; TMSB4X; KCTD13; SCML1

CRE cis-regulatory element.