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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA09g33220	A09	41865247	G	A	upstream_gene_variant	MODIFIER	c.-203G>A\|	S252
2	BAA09g33220	A09	41865947	C	T	synonymous_variant	LOW	c.498C>T\|p.Arg166Arg	S188
3	BAA09g33220	A09	41865958	G	A	missense_variant	MODERATE	c.509G>A\|p.Gly170Glu	S98
4	BAA09g33220	A09	41866004	C	T	synonymous_variant	LOW	c.555C>T\|p.Ile185Ile	S224
5	BAA09g33220	A09	41866233	C	T	missense_variant	MODERATE	c.784C>T\|p.Arg262Cys	S261 S274
6	BAA09g33220	A09	41866437	G	A	missense_variant	MODERATE	c.988G>A\|p.Ala330Thr	S249
7	BAA09g33220	A09	41866491	G	A	missense_variant	MODERATE	c.1042G>A\|p.Glu348Lys	S291
8	BAA09g33220	A09	41866711	C	T	missense_variant	MODERATE	c.1262C>T\|p.Ser421Leu	S297
9	BAA09g33220	A09	41867481	G	A	missense_variant	MODERATE	c.1943G>A\|p.Arg648Lys	S13
10	BAA09g33220	A09	41867654	G	A	missense_variant	MODERATE	c.2116G>A\|p.Asp706Asn	S105 S106
11	BAA09g33220	A09	41867707	G	A	missense_variant	MODERATE	c.2169G>A\|p.Met723Ile	S116
12	BAA09g33220	A09	41867773	C	T	synonymous_variant	LOW	c.2235C>T\|p.Ala745Ala	S246
13	BAA09g33220	A09	41870084	C	T	missense_variant	MODERATE	c.2689C>T\|p.His897Tyr	S68
14	BAA09g33220	A09	41870284	C	T	synonymous_variant	LOW	c.2889C>T\|p.Asp963Asp	S303
15	BAA09g33220	A09	41870286	C	T	missense_variant	MODERATE	c.2891C>T\|p.Ser964Leu	S32
16	BAA09g33220	A09	41870311	C	T	synonymous_variant	LOW	c.2916C>T\|p.Val972Val	S43
17	BAA09g33220	A09	41870618	G	A	missense_variant	MODERATE	c.3223G>A\|p.Gly1075Ser	S124 S127 S129 S131 S190 S223 S255 S286 S287 S57 S60
18	BAA09g33220	A09	41870635	C	T	synonymous_variant	LOW	c.3240C>T\|p.Asn1080Asn	S30 S31