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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA04g10190	A04	16414340	C	T	upstream_gene_variant	MODIFIER	c.-4800C>T\|	S10
2	BAA04g10190	A04	16415144	C	T	upstream_gene_variant	MODIFIER	c.-3996C>T\|	S8
3	BAA04g10190	A04	16415460	G	A	upstream_gene_variant	MODIFIER	c.-3680G>A\|	S177
4	BAA04g10190	A04	16415969	C	G	upstream_gene_variant	MODIFIER	c.-3171C>G\|	S115 S119 S123 S129 S138 S165 S203 S252 S266 S73
5	BAA04g10190	A04	16416374	G	A	upstream_gene_variant	MODIFIER	c.-2766G>A\|	S229
6	BAA04g10190	A04	16417978	G	A	upstream_gene_variant	MODIFIER	c.-1162G>A\|	S211 S227
7	BAA04g10190	A04	16418693	G	A	upstream_gene_variant	MODIFIER	c.-447G>A\|	S236
8	BAA04g10190	A04	16419603	C	T	missense_variant	MODERATE	c.193C>T\|p.Leu65Phe	S232
9	BAA04g10190	A04	16419695	C	T	synonymous_variant	LOW	c.285C>T\|p.Cys95Cys	S252
10	BAA04g10190	A04	16419865	G	A	synonymous_variant	LOW	c.366G>A\|p.Ala122Ala	S20
11	BAA04g10190	A04	16420465	G	A	splice_acceptor_variant&intron_variant	HIGH	c.705-1G>A\|	S120
12	BAA04g10190	A04	16421061	C	T	synonymous_variant	LOW	c.1051C>T\|p.Leu351Leu	S228
13	BAA04g10190	A04	16421800	C	T	synonymous_variant	LOW	c.1513C>T\|p.Leu505Leu	S157 S163
14	BAA04g10190	A04	16421910	C	T	splice_region_variant&intron_variant	LOW	c.1551-4C>T\|	S129
15	BAA04g10190	A04	16422727	G	A	downstream_gene_variant	MODIFIER	c.*309G>A\|	S190
16	BAA04g10190	A04	16423374	G	A	downstream_gene_variant	MODIFIER	c.*956G>A\|	S124
17	BAA04g10190	A04	16423668	G	A	downstream_gene_variant	MODIFIER	c.*1250G>A\|	S164
18	BAA04g10190	A04	16425151	C	T	downstream_gene_variant	MODIFIER	c.*2733C>T\|	S168
19	BAA04g10190	A04	16425223	C	T	downstream_gene_variant	MODIFIER	c.*2805C>T\|	S292
20	BAA04g10190	A04	16425516	G	A	downstream_gene_variant	MODIFIER	c.*3098G>A\|	S308
21	BAA04g10190	A04	16425556	C	T	downstream_gene_variant	MODIFIER	c.*3138C>T\|	S136

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