Table 1.

Genes with somatic mutations identified in this study that overlap with TCGA, Chinese, and African American CRC patient data.

Patient	Chr	Start	Stop	Reference	Alternative	Gene	Mutation	Exonic Function	Protein Change	Known
p5t	5	112174631	112174631	C	T	APC	SNV	Stop gain	p.Arg1114Ter	rs121913331, COSM13125
p10t	5	112151185	112151185	T	G	APC	SNV	Splice Region variant	-
p14t	5	112155021	112155022	TG	-	APC	deletion	Frame shift variant	p.Met431ArgfsTer12
p4low	5	112175639	112175639	C	T	APC	SNV	Stop gain	p.Arg1450Ter	rs121913332, COSM13127
p6low	5	112174249	112174249	T	A	APC	SNV	Stop gain	p.Tyr986Ter
p7low	5	112174129	112174129	A	-	APC	deletion	Frame shift variant	p.Cys947ValfsTer8
p7low	5	112175255	112175255	G	T	APC	SNV	Stop gain	p.Glu1322Ter
p10low	5	112175390	112175391	-	A	APC	Insertion	Frame shift variant	p.Thr1368AspfsTer7
p11low	5	112175639	112175639	C	T	APC	SNV	Stop gain	p.Arg1450Ter	rs121913332, COSM13127
p12low	5	112155031	112155032	-	A	APC	Insertion	Frame shift variant	p.Asn436LysfsTer8
p2t	17	7578510	7578510	G	-	TP53	Deletion	Frame shift variant	p.C141Afs*29	COSM69019
p10t	17	7576889	7576890	-	T	TP53	Insertion	Frame shift variant	p.K320Efs*17
p4t	17	70119862	70119863	-	TTCGA	SOX9	Insertion	Missense mutation	p.V291Sfs*94
p5t	17	70119855	70119856	-	CGAGA	SOX9	Insertion	Frame shift variant	p.F289Rfs*96
p10t	17	70118889	70118889	A	A	SOX9	SNV	Frame shift variant	p.F154Y
p4low	3	41274898	41274898	G	C	CTNNB1	SNV	Missense mutation	p.Trp383Ser
p13low	3	41266124	41266124	A	G	CTNNB1	SNV	Missense mutation	p.Thr41Ala	rs121913412
p14low	3	41266097	41266097	G	A	CTNNB1	SNV	Missense mutation	p.Asp32Asn	rs28931588
p14low	4	153258983	153258983	G	A	FBXW7	SNV	Stop gain	p.Arg278Ter
p14t	4	153268102	153268102	C	-	FBXW7	Deletion	Frame shift variant	p.Glu236AsnfsTer3

Chr = Chromosome.