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
176751 BAA02g18550 A02 9461967 C T upstream_gene_variant MODIFIER c.-1341C>T| S117
176752 BAA02g18550 A02 9463374 C T missense_variant MODERATE c.67C>T|p.Leu23Phe S202
176753 BAA02g18550 A02 9463384 C A missense_variant MODERATE c.77C>A|p.Ser26Tyr S270
176754 BAA02g18550 A02 9463617 G A missense_variant MODERATE c.310G>A|p.Ala104Thr S279
176755 BAA02g18560 A02 9464633 G A missense_variant MODERATE c.1844C>T|p.Ser615Phe S203
176756 BAA02g18560 A02 9464705 G A missense_variant MODERATE c.1772C>T|p.Ser591Phe S238
176757 BAA02g18560 A02 9464916 G A missense_variant MODERATE c.1646C>T|p.Ser549Phe S11
176758 BAA02g18560 A02 9465937 C T synonymous_variant LOW c.702G>A|p.Ser234Ser S94
176759 BAA02g18560 A02 9465941 G A missense_variant MODERATE c.698C>T|p.Ser233Phe S197
176760 BAA02g18560 A02 9466510 G A missense_variant MODERATE c.209C>T|p.Ser70Phe S177
176761 BAA02g18560 A02 9466857 G A upstream_gene_variant MODIFIER c.-57C>T| S86
176762 BAA02g18560 A02 9468466 G A upstream_gene_variant MODIFIER c.-1666C>T| S47
176763 BAA02g18560 A02 9468771 C T upstream_gene_variant MODIFIER c.-1971G>A| S79
S84
176764 BAA02g18560 A02 9470400 G A upstream_gene_variant MODIFIER c.-3600C>T| S264
176765 BAA02g18560 A02 9470500 G A upstream_gene_variant MODIFIER c.-3700C>T| S202
176766 BAA02g18560-BAA02g18570 A02 9472401 G A intergenic_region MODIFIER n.9472401G>A| S168
176767 BAA02g18560-BAA02g18570 A02 9472635 C T intergenic_region MODIFIER n.9472635C>T| S34
176768 BAA02g18560-BAA02g18570 A02 9473292 C T intergenic_region MODIFIER n.9473292C>T| S70
176769 BAA02g18560-BAA02g18570 A02 9475170 C T intergenic_region MODIFIER n.9475170C>T| S208
176770 BAA02g18560-BAA02g18570 A02 9477463 G A intergenic_region MODIFIER n.9477463G>A| S296
176771 BAA02g18560-BAA02g18570 A02 9477672 G A intergenic_region MODIFIER n.9477672G>A| S289
S290
176772 BAA02g18560-BAA02g18570 A02 9477841 G A intergenic_region MODIFIER n.9477841G>A| S56
176773 BAA02g18560-BAA02g18570 A02 9481426 C T intergenic_region MODIFIER n.9481426C>T| S277
176774 BAA02g18560-BAA02g18570 A02 9482786 C T intergenic_region MODIFIER n.9482786C>T| S138
176775 BAA02g18560-BAA02g18570 A02 9485130 C T intergenic_region MODIFIER n.9485130C>T| S10