Table 1.

Filtered SNV and InDel from the tumor exome.

Gene	Variation class	Variation type	Effect	AF
BRD4	Missense Mutation	SNV	p.A1243D	0.333
CCDC141	Missense Mutation	SNV	p.K992T	0.123
CDK2AP1	Missense Mutation	SNV	p.R99K	0.098
CLASP1	Missense Mutation	SNV	p.R276L	0.426
DCHS2	Missense Mutation	SNV	p.R799H	0.185
DICER1	Missense Mutation	SNV	p.E1813G	0.435
DLG5	Nonsense Mutation	SNV	p.R530*	0.394
GLG1	Splice Site	SNV	p.P147L	0.106
MTX1	Frame Shift Del	DEL	p.F157fs	0.714
NF1	Nonsense Mutation	SNV	p.R2258*	0.069
OBSL1	Missense Mutation	SNV	p.R994C	0.161
PELP1	Frame Shift Del	DEL	p.P1025fs	0.333
RBM5	Missense Mutation	SNV	p.G729S	0.457
SCARF1	Frame Shift Ins	INS	p.G303fs	0.250
SYT6	Missense Mutation	SNV	p.S404V	0.244
TAF15	Missense Mutation	SNV	p.R165L	0.420

Del: Deletion. SNV: Single Nucleotide Variation. AF: Allelic Frequency.