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


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
175751 BAA02g17990 A02 9038316 C T upstream_gene_variant MODIFIER c.-1796G>A| S242
175752 BAA02g17990 A02 9039108 G A upstream_gene_variant MODIFIER c.-2588C>T| S156
175753 BAA02g17990 A02 9039236 C T upstream_gene_variant MODIFIER c.-2716G>A| S183
S198
175754 BAA02g17990 A02 9039474 G A upstream_gene_variant MODIFIER c.-2954C>T| S159
S243
175755 BAA02g17990 A02 9039513 C T upstream_gene_variant MODIFIER c.-2993G>A| S34
175756 BAA02g17990 A02 9040537 G A upstream_gene_variant MODIFIER c.-4017C>T| S79
S91
175757 BAA02g17990 A02 9040694 G A upstream_gene_variant MODIFIER c.-4174C>T| S125
175758 BAA02g17990 A02 9041417 C T upstream_gene_variant MODIFIER c.-4897G>A| S104
S52
175759 BAA02g18000 A02 9041812 G A downstream_gene_variant MODIFIER c.*1738C>T| S174
S27
175760 BAA02g18000 A02 9041831 C T downstream_gene_variant MODIFIER c.*1719G>A| S290
175761 BAA02g18000 A02 9043507 C T downstream_gene_variant MODIFIER c.*43G>A| S266
175762 BAA02g18000 A02 9043801 C T missense_variant MODERATE c.1390G>A|p.Val464Ile S221
175763 BAA02g18000 A02 9043930 C T missense_variant MODERATE c.1261G>A|p.Asp421Asn S270
175764 BAA02g18000 A02 9045540 C T missense_variant MODERATE c.230G>A|p.Gly77Glu S75
S81
175765 BAA02g18000 A02 9045563 G A synonymous_variant LOW c.207C>T|p.Pro69Pro S170
175766 BAA02g18010 A02 9045778 C T upstream_gene_variant MODIFIER c.-4684C>T| S163
175767 BAA02g18000 A02 9048033 G A upstream_gene_variant MODIFIER c.-1359C>T| S188
175768 BAA02g18000 A02 9048085 G A upstream_gene_variant MODIFIER c.-1411C>T| S19
175769 BAA02g18000 A02 9048789 C T upstream_gene_variant MODIFIER c.-2115G>A| S166
175770 BAA02g18000 A02 9049475 C A upstream_gene_variant MODIFIER c.-2801G>T| S77
S82
175771 BAA02g18010 A02 9051207 C T missense_variant MODERATE c.188C>T|p.Ala63Val S246
175772 BAA02g18010 A02 9051424 G A splice_acceptor_variant&intron_variant HIGH c.242-1G>A| S60
175773 BAA02g18010 A02 9051498 G A synonymous_variant LOW c.315G>A|p.Leu105Leu S247
175774 BAA02g18010 A02 9051770 C T synonymous_variant LOW c.423C>T|p.Tyr141Tyr S40
S49
175775 BAA02g18020 A02 9052423 C T downstream_gene_variant MODIFIER c.*2105G>A| S289
S290