Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA02g35310	A02	30355304	C	T	upstream_gene_variant	MODIFIER	c.-4366C>T\|	S242
2	BAA02g35310	A02	30355369	C	T	upstream_gene_variant	MODIFIER	c.-4301C>T\|	S216
3	BAA02g35310	A02	30355622	C	T	upstream_gene_variant	MODIFIER	c.-4048C>T\|	S173 S176
4	BAA02g35310	A02	30355658	C	T	upstream_gene_variant	MODIFIER	c.-4012C>T\|	S15
5	BAA02g35310	A02	30355974	C	T	upstream_gene_variant	MODIFIER	c.-3696C>T\|	S194
6	BAA02g35310	A02	30355982	G	A	upstream_gene_variant	MODIFIER	c.-3688G>A\|	S298
7	BAA02g35310	A02	30356008	C	T	upstream_gene_variant	MODIFIER	c.-3662C>T\|	S18
8	BAA02g35310	A02	30356437	G	A	upstream_gene_variant	MODIFIER	c.-3233G>A\|	S215
9	BAA02g35310	A02	30356517	G	A	upstream_gene_variant	MODIFIER	c.-3153G>A\|	S281
10	BAA02g35310	A02	30358183	G	A	upstream_gene_variant	MODIFIER	c.-1487G>A\|	S34
11	BAA02g35310	A02	30360696	G	C	missense_variant	MODERATE	c.792G>C\|p.Glu264Asp	S108 S112 S120 S127 S132 S17 S235 S258 S31 S34 S69 S76 S92
12	BAA02g35310	A02	30362645	G	A	missense_variant	MODERATE	c.1973G>A\|p.Gly658Glu	S37
13	BAA02g35310	A02	30363162	G	A	stop_gained	HIGH	c.2379G>A\|p.Trp793*	S10
14	BAA02g35310	A02	30363248	C	T	missense_variant	MODERATE	c.2465C>T\|p.Ala822Val	S221
15	BAA02g35310	A02	30363392	C	T	downstream_gene_variant	MODIFIER	c.*38C>T\|	S139
16	BAA02g35310	A02	30363694	G	A	downstream_gene_variant	MODIFIER	c.*340G>A\|	S28