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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
145751	BAA10g30220	A10	22492077	G	A	missense_variant	MODERATE	c.307G>A\|p.Glu103Lys	S270
145752	BAA10g30220	A10	22492162	G	A	missense_variant	MODERATE	c.392G>A\|p.Gly131Glu	S122
145753	BAA10g30220	A10	22493111	G	A	missense_variant	MODERATE	c.1021G>A\|p.Gly341Arg	S151 S167 S236 S257 S262 S263
145754	BAA10g30220	A10	22493137	C	T	synonymous_variant	LOW	c.1047C>T\|p.Tyr349Tyr	S10
145755	BAA10g30220	A10	22493491	G	A	missense_variant	MODERATE	c.1163G>A\|p.Gly388Glu	S197
145756	BAA10g30220	A10	22493567	C	T	synonymous_variant	LOW	c.1239C>T\|p.Ser413Ser	S155 S211
145757	BAA10g30220	A10	22493639	C	T	synonymous_variant	LOW	c.1311C>T\|p.Ser437Ser	S105
145758	BAA10g30220	A10	22494490	G	A	missense_variant	MODERATE	c.1860G>A\|p.Met620Ile	S263
145759	BAA10g30220	A10	22495361	G	A	missense_variant	MODERATE	c.2483G>A\|p.Arg828Lys	S54
145760	BAA10g30230	A10	22495905	C	T	upstream_gene_variant	MODIFIER	c.-1211C>T\|	S25 S265
145761	BAA10g30230	A10	22496817	C	T	upstream_gene_variant	MODIFIER	c.-299C>T\|	S123
145762	BAA10g30230	A10	22496857	C	T	upstream_gene_variant	MODIFIER	c.-259C>T\|	S73 S91
145763	BAA10g30230	A10	22497275	C	T	splice_region_variant&intron_variant	LOW	c.156+4C>T\|	S246
145764	BAA10g30230	A10	22497362	C	T	missense_variant	MODERATE	c.170C>T\|p.Ala57Val	S211 S227
145765	BAA10g30230	A10	22497799	G	A	missense_variant	MODERATE	c.397G>A\|p.Glu133Lys	S59
145766	BAA10g30230	A10	22498712	G	A	stop_gained	HIGH	c.747G>A\|p.Trp249*	S298
145767	BAA10g30230	A10	22498995	C	T	synonymous_variant	LOW	c.873C>T\|p.Asp291Asp	S115
145768	BAA10g30230	A10	22499605	C	T	synonymous_variant	LOW	c.1254C>T\|p.Asn418Asn	S152
145769	BAA10g30230	A10	22499959	G	A	missense_variant&splice_region_variant	MODERATE	c.1447G>A\|p.Asp483Asn	S174
145770	BAA10g30240	A10	22502295	C	T	upstream_gene_variant	MODIFIER	c.-4823C>T\|	S306 S308
145771	BAA10g30240	A10	22502590	C	T	upstream_gene_variant	MODIFIER	c.-4528C>T\|	S13
145772	BAA10g30240	A10	22505029	G	A	upstream_gene_variant	MODIFIER	c.-2089G>A\|	S212
145773	BAA10g30240	A10	22505707	C	T	upstream_gene_variant	MODIFIER	c.-1411C>T\|	S152
145774	BAA10g30240	A10	22506766	G	A	upstream_gene_variant	MODIFIER	c.-352G>A\|	S33
145775	BAA10g30240	A10	22506846	G	A	upstream_gene_variant	MODIFIER	c.-272G>A\|	S216

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