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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
95701	BAA10g04230	A10	2119851	G	A	missense_variant	MODERATE	c.1048G>A\|p.Glu350Lys	S109
95702	BAA10g04230	A10	2119998	G	A	missense_variant	MODERATE	c.1195G>A\|p.Glu399Lys	S136
95703	BAA10g04240	A10	2120737	G	A	upstream_gene_variant	MODIFIER	c.-1337G>A\|	S157 S163
95704	BAA10g04230	A10	2120790	C	T	missense_variant	MODERATE	c.1847C>T\|p.Ser616Leu	S294
95705	BAA10g04230	A10	2121288	C	T	stop_gained	HIGH	c.2152C>T\|p.Arg718*	S142
95706	BAA10g04230	A10	2122742	G	A	downstream_gene_variant	MODIFIER	c.*1320G>A\|	S77 S82
95707	BAA10g04230	A10	2122810	G	A	downstream_gene_variant	MODIFIER	c.*1388G>A\|	S205
95708	BAA10g04230	A10	2123216	G	A	downstream_gene_variant	MODIFIER	c.*1794G>A\|	S157 S163 S226
95709	BAA10g04230	A10	2123651	G	A	downstream_gene_variant	MODIFIER	c.*2229G>A\|	S180
95710	BAA10g04230	A10	2123892	C	T	downstream_gene_variant	MODIFIER	c.*2470C>T\|	S203
95711	BAA10g04230	A10	2124389	G	A	downstream_gene_variant	MODIFIER	c.*2967G>A\|	S13
95712	BAA10g04230	A10	2125120	G	A	downstream_gene_variant	MODIFIER	c.*3698G>A\|	S99
95713	BAA10g04250	A10	2128823	G	A	upstream_gene_variant	MODIFIER	c.-2607C>T\|	S109
95714	BAA10g04260	A10	2131920	C	T	upstream_gene_variant	MODIFIER	c.-484G>A\|	S259
95715	BAA10g04260	A10	2132055	G	A	upstream_gene_variant	MODIFIER	c.-619C>T\|	S60
95716	BAA10g04290	A10	2156309	T	A	upstream_gene_variant	MODIFIER	c.-3008T>A\|	S303 S6
95717	BAA10g04290	A10	2157860	G	A	upstream_gene_variant	MODIFIER	c.-1457G>A\|	S20
95718	BAA10g04290	A10	2158054	G	A	upstream_gene_variant	MODIFIER	c.-1263G>A\|	S164
95719	BAA10g04290	A10	2158536	C	T	upstream_gene_variant	MODIFIER	c.-781C>T\|	S263
95720	BAA10g04300	A10	2160679	C	T	missense_variant	MODERATE	c.1510G>A\|p.Asp504Asn	S89
95721	BAA10g04300	A10	2160711	C	T	stop_gained	HIGH	c.1478G>A\|p.Trp493*	S135
95722	BAA10g04300	A10	2160900	C	T	missense_variant&splice_region_variant	MODERATE	c.1453G>A\|p.Ala485Thr	S281
95723	BAA10g04300	A10	2161024	C	T	splice_acceptor_variant&intron_variant	HIGH	c.1330-1G>A\|	S246
95724	BAA10g04290	A10	2161103	C	T	downstream_gene_variant	MODIFIER	c.*941C>T\|	S95
95725	BAA10g04290	A10	2161220	G	A	downstream_gene_variant	MODIFIER	c.*1058G>A\|	S262

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