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
164151 BAA02g10710 A02 4786747 C T upstream_gene_variant MODIFIER c.-4124G>A| S250
164152 BAA02g10710 A02 4787521 C T upstream_gene_variant MODIFIER c.-4898G>A| S293
164153 BAA02g10720 A02 4787662 G A downstream_gene_variant MODIFIER c.*1164C>T| S95
164154 BAA02g10720 A02 4791757 C T upstream_gene_variant MODIFIER c.-109G>A| S179
164155 BAA02g10720 A02 4792631 C T upstream_gene_variant MODIFIER c.-983G>A| S112
164156 BAA02g10720 A02 4793651 G A upstream_gene_variant MODIFIER c.-2003C>T| S246
164157 BAA02g10720 A02 4794056 C T upstream_gene_variant MODIFIER c.-2408G>A| S46
164158 BAA02g10720 A02 4794302 G A upstream_gene_variant MODIFIER c.-2654C>T| S208
164159 BAA02g10720 A02 4794308 C T upstream_gene_variant MODIFIER c.-2660G>A| S67
164160 BAA02g10730 A02 4796764 G A downstream_gene_variant MODIFIER c.*810C>T| S125
164161 BAA02g10730 A02 4797171 G A downstream_gene_variant MODIFIER c.*403C>T| S303
164162 BAA02g10730 A02 4797421 G A downstream_gene_variant MODIFIER c.*153C>T| S188
164163 BAA02g10730 A02 4799246 G A splice_region_variant&intron_variant LOW c.445+7C>T| S35
164164 BAA02g10730 A02 4799537 A G intron_variant MODIFIER c.388-227T>C| S82
S92
164165 BAA02g10730 A02 4800481 C T upstream_gene_variant MODIFIER c.-74G>A| S116
164166 BAA02g10730 A02 4802762 G A upstream_gene_variant MODIFIER c.-2355C>T| S206
S26
164167 BAA02g10730 A02 4804004 G A upstream_gene_variant MODIFIER c.-3597C>T| S132
S137
164168 BAA02g10740 A02 4806326 G A downstream_gene_variant MODIFIER c.*901C>T| S139
164169 BAA02g10740 A02 4806972 G A downstream_gene_variant MODIFIER c.*255C>T| S172
S202
S217
164170 BAA02g10740 A02 4807571 G A intron_variant MODIFIER c.979+88C>T| S133
164171 BAA02g10740 A02 4807966 G A missense_variant MODERATE c.833C>T|p.Thr278Ile S107
164172 BAA02g10740 A02 4808613 C T intron_variant MODIFIER c.600+210G>A| S67
164173 BAA02g10740 A02 4808965 C T intron_variant MODIFIER c.486-28G>A| S283
164174 BAA02g10740 A02 4810259 G A missense_variant MODERATE c.7C>T|p.Leu3Phe S164
164175 BAA02g10740 A02 4812276 G A upstream_gene_variant MODIFIER c.-2011C>T| S27