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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA06g22770	A06	12706251	C	T	downstream_gene_variant	MODIFIER	c.*4302G>A\|	S286
2	BAA06g22770	A06	12706773	G	A	downstream_gene_variant	MODIFIER	c.*3780C>T\|	S135 S152 S185 S273
3	BAA06g22770	A06	12708436	C	T	downstream_gene_variant	MODIFIER	c.*2117G>A\|	S294
4	BAA06g22770	A06	12708765	G	A	downstream_gene_variant	MODIFIER	c.*1788C>T\|	S190
5	BAA06g22770	A06	12709101	G	A	downstream_gene_variant	MODIFIER	c.*1452C>T\|	S237
6	BAA06g22770	A06	12709315	G	A	downstream_gene_variant	MODIFIER	c.*1238C>T\|	S100
7	BAA06g22770	A06	12709399	G	A	downstream_gene_variant	MODIFIER	c.*1154C>T\|	S146
8	BAA06g22770	A06	12709888	G	A	downstream_gene_variant	MODIFIER	c.*665C>T\|	S274
9	BAA06g22770	A06	12710819	C	T	synonymous_variant	LOW	c.807G>A\|p.Glu269Glu	S186 S47
10	BAA06g22770	A06	12710836	G	A	missense_variant	MODERATE	c.790C>T\|p.Pro264Ser	S289 S290
11	BAA06g22770	A06	12711108	G	A	intron_variant	MODIFIER	c.548-30C>T\|	S70
12	BAA06g22770	A06	12711245	C	T	intron_variant	MODIFIER	c.548-167G>A\|	S293
13	BAA06g22770	A06	12711397	C	T	intron_variant	MODIFIER	c.548-319G>A\|	S276
14	BAA06g22770	A06	12712498	C	T	missense_variant	MODERATE	c.269G>A\|p.Arg90His	S298
15	BAA06g22770	A06	12712526	C	T	missense_variant	MODERATE	c.241G>A\|p.Gly81Arg	S233
16	BAA06g22770	A06	12714218	C	T	upstream_gene_variant	MODIFIER	c.-1358G>A\|	S43
17	BAA06g22770	A06	12716143	C	T	upstream_gene_variant	MODIFIER	c.-3283G>A\|	S87
18	BAA06g22770	A06	12716719	G	T	upstream_gene_variant	MODIFIER	c.-3859C>A\|	S100 S105 S107 S108 S17 S171 S177 S206 S213 S227 S247 S270 S274 S284 S36 S39 S70 S79 S93
19	BAA06g22770	A06	12717363	G	A	upstream_gene_variant	MODIFIER	c.-4503C>T\|	S262
20	BAA06g22770	A06	12717503	G	A	upstream_gene_variant	MODIFIER	c.-4643C>T\|	S129

Users can query the SNP information according to the gene ID.