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
176101 BAA02g18210 A02 9175209 G A upstream_gene_variant MODIFIER c.-4298G>A| S232
176102 BAA02g18210 A02 9175364 G A upstream_gene_variant MODIFIER c.-4143G>A| S286
176103 BAA02g18210 A02 9175616 C T upstream_gene_variant MODIFIER c.-3891C>T| S278
176104 BAA02g18210 A02 9176230 G A upstream_gene_variant MODIFIER c.-3277G>A| S238
176105 BAA02g18210 A02 9177096 G A upstream_gene_variant MODIFIER c.-2411G>A| S187
176106 BAA02g18210 A02 9180401 C T missense_variant MODERATE c.895C>T|p.Leu299Phe S283
176107 BAA02g18210 A02 9182789 G A downstream_gene_variant MODIFIER c.*1759G>A| S188
176108 BAA02g18210 A02 9183634 G A downstream_gene_variant MODIFIER c.*2604G>A| S287
176109 BAA02g18220 A02 9185847 G A upstream_gene_variant MODIFIER c.-1018C>T| S60
176110 BAA02g18220 A02 9186474 C T upstream_gene_variant MODIFIER c.-1645G>A| S272
176111 BAA02g18220 A02 9186503 C T upstream_gene_variant MODIFIER c.-1674G>A| S156
S34
176112 BAA02g18220 A02 9186879 C T upstream_gene_variant MODIFIER c.-2050G>A| S128
176113 BAA02g18220 A02 9189021 G A upstream_gene_variant MODIFIER c.-4192C>T| S76
176114 BAA02g18220 A02 9189245 C T upstream_gene_variant MODIFIER c.-4416G>A| S38
176115 BAA02g18230 A02 9190085 G A intron_variant MODIFIER c.122-389G>A| S95
176116 BAA02g18230 A02 9190351 C T intron_variant MODIFIER c.122-123C>T| S201
176117 BAA02g18230 A02 9191014 G A missense_variant MODERATE c.571G>A|p.Glu191Lys S297
176118 BAA02g18230 A02 9191110 G A missense_variant MODERATE c.667G>A|p.Glu223Lys S156
176119 BAA02g18230 A02 9191380 G A downstream_gene_variant MODIFIER c.*187G>A| S153
S213
176120 BAA02g18230 A02 9191631 G A downstream_gene_variant MODIFIER c.*438G>A| S148
S210
S30
S31
176121 BAA02g18230 A02 9192021 G A downstream_gene_variant MODIFIER c.*828G>A| S60
176122 BAA02g18230 A02 9194462 C T downstream_gene_variant MODIFIER c.*3269C>T| S182
176123 BAA02g18240 A02 9196683 C T downstream_gene_variant MODIFIER c.*2492G>A| S32
176124 BAA02g18240 A02 9204218 G A upstream_gene_variant MODIFIER c.-961C>T| S298
176125 BAA02g18240 A02 9205888 C T upstream_gene_variant MODIFIER c.-2631G>A| S100