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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA10g05350	A10	2740254	G	A	synonymous_variant	LOW	c.204G>A\|p.Glu68Glu	S13
2	BAA10g05350	A10	2740963	C	T	missense_variant	MODERATE	c.490C>T\|p.Pro164Ser	S132 S137 S215 S89
3	BAA10g05350	A10	2741425	G	A	missense_variant	MODERATE	c.763G>A\|p.Val255Ile	S292
4	BAA10g05350	A10	2741813	G	A	intron_variant	MODIFIER	c.959+11G>A\|	S268
5	BAA10g05350	A10	2744370	G	A	intron_variant	MODIFIER	c.2074-40G>A\|	S198
6	BAA10g05350	A10	2744569	G	A	splice_acceptor_variant&intron_variant	HIGH	c.2156-1G>A\|	S9
7	BAA10g05350	A10	2745128	G	A	missense_variant	MODERATE	c.2401G>A\|p.Glu801Lys	S167
8	BAA10g05350	A10	2745312	G	A	splice_acceptor_variant&intron_variant	HIGH	c.2493-1G>A\|	S150
9	BAA10g05350	A10	2745738	C	T	intron_variant	MODIFIER	c.2739-20C>T\|	S60
10	BAA10g05350	A10	2746736	G	A	missense_variant	MODERATE	c.3268G>A\|p.Glu1090Lys	S33
11	BAA10g05350	A10	2747559	G	A	splice_acceptor_variant&intron_variant	HIGH	c.3702-1G>A\|	S7
12	BAA10g05350	A10	2749042	C	T	synonymous_variant	LOW	c.4558C>T\|p.Leu1520Leu	S270
13	BAA10g05350	A10	2749049	G	A	missense_variant	MODERATE	c.4565G>A\|p.Ser1522Asn	S148 S210 S30 S31
14	BAA10g05350	A10	2750163	C	T	missense_variant	MODERATE	c.5498C>T\|p.Thr1833Ile	S226
15	BAA10g05350	A10	2750729	C	T	downstream_gene_variant	MODIFIER	c.*204C>T\|	S67