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
169801 BAA02g14790 A02 6980139 C T upstream_gene_variant MODIFIER c.-1435G>A| S272
169802 BAA02g14790 A02 6980174 C T upstream_gene_variant MODIFIER c.-1470G>A| S202
169803 BAA02g14790 A02 6980377 C T upstream_gene_variant MODIFIER c.-1673G>A| S230
169804 BAA02g14790 A02 6980431 C T upstream_gene_variant MODIFIER c.-1727G>A| S211
S227
169805 BAA02g14790 A02 6982030 C T upstream_gene_variant MODIFIER c.-3326G>A| S79
169806 BAA02g14790 A02 6982557 G A upstream_gene_variant MODIFIER c.-3853C>T| S206
169807 BAA02g14790 A02 6982699 G A upstream_gene_variant MODIFIER c.-3995C>T| S13
S168
S279
S64
169808 BAA02g14790 A02 6983475 C T upstream_gene_variant MODIFIER c.-4771G>A| S194
169809 BAA02g14800 A02 6983763 G A upstream_gene_variant MODIFIER c.-608G>A| S293
169810 BAA02g14800 A02 6984389 G A missense_variant MODERATE c.19G>A|p.Asp7Asn S291
169811 BAA02g14800 A02 6984558 C T missense_variant MODERATE c.188C>T|p.Ser63Phe S270
169812 BAA02g14800 A02 6984999 G A synonymous_variant LOW c.213G>A|p.Ala71Ala S205
169813 BAA02g14800 A02 6985213 C T synonymous_variant LOW c.427C>T|p.Leu143Leu S185
169814 BAA02g14800 A02 6985334 C T missense_variant MODERATE c.548C>T|p.Ser183Phe S308
169815 BAA02g14800 A02 6985798 C T missense_variant MODERATE c.943C>T|p.Pro315Ser S34
169816 BAA02g14800 A02 6985807 C T missense_variant MODERATE c.952C>T|p.Pro318Ser S79
S84
169817 BAA02g14800 A02 6986340 G A synonymous_variant LOW c.1332G>A|p.Glu444Glu S162
169818 BAA02g14800 A02 6986851 G A missense_variant MODERATE c.1843G>A|p.Glu615Lys S10
169819 BAA02g14820 A02 6987687 G A upstream_gene_variant MODIFIER c.-4124G>A| S69
169820 BAA02g14810 A02 6990142 G A upstream_gene_variant MODIFIER c.-298C>T| S4
169821 BAA02g14810 A02 6990451 G A upstream_gene_variant MODIFIER c.-607C>T| S153
S213
169822 BAA02g14810 A02 6990622 C T upstream_gene_variant MODIFIER c.-778G>A| S174
S27
169823 BAA02g14810 A02 6990661 G A upstream_gene_variant MODIFIER c.-817C>T| S289
S290
169824 BAA02g14810 A02 6990854 C T upstream_gene_variant MODIFIER c.-1010G>A| S202
169825 BAA02g14810 A02 6991177 G A upstream_gene_variant MODIFIER c.-1333C>T| S188