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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g13040 A02 5838464 G A upstream_gene_variant MODIFIER c.-4115G>A| S98
2 BAA02g13040 A02 5838880 G A upstream_gene_variant MODIFIER c.-3699G>A| S302
3 BAA02g13040 A02 5839081 C T upstream_gene_variant MODIFIER c.-3498C>T| S209
4 BAA02g13040 A02 5839123 C T upstream_gene_variant MODIFIER c.-3456C>T| S185
5 BAA02g13040 A02 5839265 C T upstream_gene_variant MODIFIER c.-3314C>T| S44
6 BAA02g13040 A02 5839298 G A upstream_gene_variant MODIFIER c.-3281G>A| S291
7 BAA02g13040 A02 5840118 C T upstream_gene_variant MODIFIER c.-2461C>T| S252
8 BAA02g13040 A02 5841207 C T upstream_gene_variant MODIFIER c.-1372C>T| S289
S290
9 BAA02g13040 A02 5841714 C T upstream_gene_variant MODIFIER c.-865C>T| S138
10 BAA02g13040 A02 5841750 G A upstream_gene_variant MODIFIER c.-829G>A| S105
S106
11 BAA02g13040 A02 5841992 C T upstream_gene_variant MODIFIER c.-587C>T| S200
12 BAA02g13040 A02 5844988 G A downstream_gene_variant MODIFIER c.*2203G>A| S289
S290
13 BAA02g13040 A02 5846318 A T downstream_gene_variant MODIFIER c.*3533A>T| S197
14 BAA02g13040 A02 5847471 C T downstream_gene_variant MODIFIER c.*4686C>T| S292