Hugo_Symbol	Gene_Symbol	Ensembl_ID	Chromosome	Start_Position	End_Position	Variant_Classification	Variant_Type	Reference_Allele	Tumor_Seq_Allele	Tumor_Sample_Barcode	HGVSp_Short	Variant	Pathogenicity	Mutation_Status	VAF
KRAS	KRAS	ENSG00000133703	12	25398284	25398284	Missense_Mutation	SNP	C	A	PAAD-SAMPLE-001	p.G12V	c.35G>T	Pathogenic	Somatic	0.48
TP53	TP53	ENSG00000141510	17	7674220	7674220	Missense_Mutation	SNP	C	T	PAAD-SAMPLE-001	p.R248W	c.742C>T	Pathogenic	Somatic	0.44
SMAD4	SMAD4	ENSG00000141646	18	48591918	48591918	Nonsense_Mutation	SNP	C	T	PAAD-SAMPLE-001	p.R361*	c.1081C>T	Pathogenic	Somatic	0.39
CDKN2A	CDKN2A	ENSG00000147889	9	21971186	21971186	Nonsense_Mutation	SNP	G	T	PAAD-SAMPLE-001	p.R58*	c.172C>A	Pathogenic	Somatic	0.35
RNF43	RNF43	ENSG00000108375	17	56397431	56397434	Frameshift_Del	DEL	GCTT	-	PAAD-SAMPLE-001	p.G659fs	c.1975_1978delGCTT	Pathogenic	Somatic	0.21
MUC16	MUC16	ENSG00000181143	19	9042526	9042526	Missense_Mutation	SNP	A	G	PAAD-SAMPLE-001	p.S11977G	c.35930A>G	Likely Pathogenic	Somatic	0.18
TTN	TTN	ENSG00000155657	2	179393004	179393004	Missense_Mutation	SNP	G	A	PAAD-SAMPLE-001	p.R14167Q	c.42500G>A	Variant of Uncertain Significance	Somatic	0.15
ARID1A	ARID1A	ENSG00000117713	1	26780603	26780606	Frameshift_Del	DEL	ACTT	-	PAAD-SAMPLE-001	p.L1518fs	c.4552_4555delACTT	Pathogenic	Somatic	0.12