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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA04g02260	A04	1333652	G	A	missense_variant	MODERATE	c.2894C>T\|p.Ser965Phe	S57
2	BAA04g02260	A04	1333729	C	T	stop_gained	HIGH	c.2817G>A\|p.Trp939*	S180
3	BAA04g02260	A04	1334298	C	T	missense_variant	MODERATE	c.2248G>A\|p.Val750Met	S237
4	BAA04g02260	A04	1334424	C	T	missense_variant	MODERATE	c.2122G>A\|p.Val708Met	S127 S190 S223 S286 S287 S57
5	BAA04g02260	A04	1334682	C	T	missense_variant	MODERATE	c.1864G>A\|p.Glu622Lys	S200
6	BAA04g02260	A04	1335021	G	A	synonymous_variant	LOW	c.1525C>T\|p.Leu509Leu	S133
7	BAA04g02260	A04	1335224	G	A	missense_variant	MODERATE	c.1322C>T\|p.Ser441Phe	S51
8	BAA04g02260	A04	1336288	G	A	synonymous_variant	LOW	c.258C>T\|p.His86His	S251
9	BAA04g02260	A04	1336467	C	T	missense_variant	MODERATE	c.79G>A\|p.Asp27Asn	S19
10	BAA04g02260	A04	1336969	C	T	upstream_gene_variant	MODIFIER	c.-424G>A\|	S172
11	BAA04g02260	A04	1338003	C	T	upstream_gene_variant	MODIFIER	c.-1458G>A\|	S15 S156 S3 S34 S6
12	BAA04g02260	A04	1338552	C	T	upstream_gene_variant	MODIFIER	c.-2007G>A\|	S45
13	BAA04g02260	A04	1339215	G	A	upstream_gene_variant	MODIFIER	c.-2670C>T\|	S11
14	BAA04g02260	A04	1339965	C	T	upstream_gene_variant	MODIFIER	c.-3420G>A\|	S129
15	BAA04g02260	A04	1340105	C	T	upstream_gene_variant	MODIFIER	c.-3560G>A\|	S204