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
175601 BAA02g17900 A02 8988544 G A upstream_gene_variant MODIFIER c.-3617C>T| S197
175602 BAA02g17900 A02 8988983 G A upstream_gene_variant MODIFIER c.-4056C>T| S193
175603 BAA02g17900-BAA02g17910 A02 8990064 G A intergenic_region MODIFIER n.8990064G>A| S37
175604 BAA02g17900-BAA02g17910 A02 8991312 C T intergenic_region MODIFIER n.8991312C>T| S275
175605 BAA02g17900-BAA02g17910 A02 8992858 G A intergenic_region MODIFIER n.8992858G>A| S168
175606 BAA02g17900-BAA02g17910 A02 8993006 G A intergenic_region MODIFIER n.8993006G>A| S118
175607 BAA02g17900-BAA02g17910 A02 8993846 G A intergenic_region MODIFIER n.8993846G>A| S256
175608 BAA02g17900-BAA02g17910 A02 8994519 G A intergenic_region MODIFIER n.8994519G>A| S173
175609 BAA02g17910 A02 8996413 G A downstream_gene_variant MODIFIER c.*3366C>T| S236
175610 BAA02g17910 A02 8996678 C T downstream_gene_variant MODIFIER c.*3101G>A| S63
175611 BAA02g17910 A02 8997314 G A downstream_gene_variant MODIFIER c.*2465C>T| S11
175612 BAA02g17910 A02 8997842 G A downstream_gene_variant MODIFIER c.*1937C>T| S69
175613 BAA02g17920 A02 9000184 C T downstream_gene_variant MODIFIER c.*2206G>A| S128
175614 BAA02g17920 A02 9000232 G A downstream_gene_variant MODIFIER c.*2158C>T| S146
175615 BAA02g17910 A02 9000471 C T synonymous_variant LOW c.297G>A|p.Leu99Leu S138
175616 BAA02g17910 A02 9004132 G A upstream_gene_variant MODIFIER c.-3365C>T| S67
175617 BAA02g17910 A02 9004268 G A upstream_gene_variant MODIFIER c.-3501C>T| S223
175618 BAA02g17910 A02 9004880 G A upstream_gene_variant MODIFIER c.-4113C>T| S51
175619 BAA02g17910 A02 9005168 G A upstream_gene_variant MODIFIER c.-4401C>T| S190
175620 BAA02g17920 A02 9006269 C T upstream_gene_variant MODIFIER c.-2424G>A| S201
175621 BAA02g17920 A02 9007663 C T upstream_gene_variant MODIFIER c.-3818G>A| S18
175622 BAA02g17930 A02 9008238 G A missense_variant MODERATE c.92C>T|p.Ser31Phe S274
175623 BAA02g17920 A02 9008745 C T upstream_gene_variant MODIFIER c.-4900G>A| S112
175624 BAA02g17940 A02 9009714 C T upstream_gene_variant MODIFIER c.-2125C>T| S119
175625 BAA02g17940 A02 9010293 C T upstream_gene_variant MODIFIER c.-1546C>T| S44