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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
87801	BAA01g46790	A01	31168803	C	T	missense_variant	MODERATE	c.346G>A\|p.Glu116Lys	S56
87802	BAA01g46790	A01	31168862	C	T	missense_variant	MODERATE	c.287G>A\|p.Gly96Glu	S74
87803	BAA01g46790	A01	31169065	G	A	synonymous_variant	LOW	c.84C>T\|p.Ile28Ile	S115
87804	BAA01g46800	A01	31170041	C	T	missense_variant	MODERATE	c.575C>T\|p.Ser192Leu	S73 S91
87805	BAA01g46800	A01	31170498	G	A	synonymous_variant	LOW	c.1032G>A\|p.Glu344Glu	S264
87806	BAA01g46800	A01	31170652	G	A	missense_variant	MODERATE	c.1186G>A\|p.Val396Met	S100
87807	BAA01g46800	A01	31170895	C	T	missense_variant	MODERATE	c.1429C>T\|p.Arg477Cys	S133
87808	BAA01g46800	A01	31171104	T	A	missense_variant	MODERATE	c.1638T>A\|p.Asn546Lys	S103 S131 S215 S228 S269 S53
87809	BAA01g46800	A01	31171323	G	A	synonymous_variant	LOW	c.1857G>A\|p.Gln619Gln	S149
87810	BAA01g46810	A01	31172606	C	T	missense_variant	MODERATE	c.1723G>A\|p.Asp575Asn	S69
87811	BAA01g46810	A01	31172811	C	T	synonymous_variant	LOW	c.1518G>A\|p.Arg506Arg	S8
87812	BAA01g46810	A01	31172826	C	T	synonymous_variant	LOW	c.1503G>A\|p.Ala501Ala	S292
87813	BAA01g46810	A01	31173170	G	A	missense_variant	MODERATE	c.1337C>T\|p.Thr446Ile	S34
87814	BAA01g46810	A01	31173592	G	A	missense_variant	MODERATE	c.1006C>T\|p.Pro336Ser	S298
87815	BAA01g46810	A01	31173853	G	A	missense_variant	MODERATE	c.935C>T\|p.Ser312Phe	S135 S273 S68
87816	BAA01g46810	A01	31174105	C	T	splice_acceptor_variant&intron_variant	HIGH	c.778-1G>A\|	S184
87817	BAA01g46820	A01	31174900	C	T	upstream_gene_variant	MODIFIER	c.-3626C>T\|	S39
87818	BAA01g46820	A01	31175381	C	T	upstream_gene_variant	MODIFIER	c.-3145C>T\|	S112
87819	BAA01g46810	A01	31177731	C	T	upstream_gene_variant	MODIFIER	c.-2242G>A\|	S166
87820	BAA01g46810	A01	31178078	G	A	upstream_gene_variant	MODIFIER	c.-2589C>T\|	S107
87821	BAA01g46810	A01	31178755	C	T	upstream_gene_variant	MODIFIER	c.-3266G>A\|	S15 S156 S3 S34 S4 S6
87822	BAA01g46810	A01	31178956	G	A	upstream_gene_variant	MODIFIER	c.-3467C>T\|	S279
87823	BAA01g46810	A01	31179248	T	C	upstream_gene_variant	MODIFIER	c.-3759A>G\|	S115 S117 S121 S122 S23 S266 S297 S55 S65 S8
87824	BAA01g46820	A01	31179727	C	T	missense_variant	MODERATE	c.355C>T\|p.Pro119Ser	S233
87825	BAA01g46810	A01	31179853	G	A	upstream_gene_variant	MODIFIER	c.-4364C>T\|	S87

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