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
195201 BAA02g28420 A02 15969374 C T downstream_gene_variant MODIFIER c.*4394C>T| S175
195202 BAA02g28420-BAA02g28430 A02 15970557 G A intergenic_region MODIFIER n.15970557G>A| S298
195203 BAA02g28420-BAA02g28430 A02 15970693 G A intergenic_region MODIFIER n.15970693G>A| S150
195204 BAA02g28420-BAA02g28430 A02 15970799 C T intergenic_region MODIFIER n.15970799C>T| S224
S242
195205 BAA02g28420-BAA02g28430 A02 15971638 C T intergenic_region MODIFIER n.15971638C>T| S8
195206 BAA02g28420-BAA02g28430 A02 15971690 C T intergenic_region MODIFIER n.15971690C>T| S107
195207 BAA02g28420-BAA02g28430 A02 15973423 T A intergenic_region MODIFIER n.15973423T>A| S181
195208 BAA02g28420-BAA02g28430 A02 15973598 G A intergenic_region MODIFIER n.15973598G>A| S166
195209 BAA02g28430 A02 15974163 G A downstream_gene_variant MODIFIER c.*4703C>T| S133
195210 BAA02g28430 A02 15974178 G A downstream_gene_variant MODIFIER c.*4688C>T| S148
S30
S31
195211 BAA02g28430 A02 15975446 G A downstream_gene_variant MODIFIER c.*3420C>T| S62
195212 BAA02g28430 A02 15975857 C T downstream_gene_variant MODIFIER c.*3009G>A| S202
195213 BAA02g28430 A02 15977516 G A downstream_gene_variant MODIFIER c.*1350C>T| S228
195214 BAA02g28430 A02 15978035 C T downstream_gene_variant MODIFIER c.*831G>A| S81
195215 BAA02g28430 A02 15978684 G A downstream_gene_variant MODIFIER c.*182C>T| S217
S248
195216 BAA02g28430 A02 15979414 G A synonymous_variant LOW c.1215C>T|p.Tyr405Tyr S169
195217 BAA02g28430 A02 15980074 C T missense_variant MODERATE c.1082G>A|p.Arg361Lys S296
195218 BAA02g28430 A02 15980221 C T splice_region_variant&intron_variant LOW c.1024-4G>A| S152
195219 BAA02g28430 A02 15981175 G A missense_variant MODERATE c.500C>T|p.Thr167Ile S186
195220 BAA02g28430 A02 15981587 G A missense_variant MODERATE c.88C>T|p.Leu30Phe S169
195221 BAA02g28430 A02 15981601 C T missense_variant MODERATE c.74G>A|p.Arg25His S218
195222 BAA02g28430 A02 15981940 G A upstream_gene_variant MODIFIER c.-266C>T| S197
195223 BAA02g28430 A02 15982563 C T upstream_gene_variant MODIFIER c.-889G>A| S174
195224 BAA02g28430 A02 15982573 G A upstream_gene_variant MODIFIER c.-899C>T| S297
195225 BAA02g28430 A02 15982676 G A upstream_gene_variant MODIFIER c.-1002C>T| S7