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
40801 BAA01g25780 A01 14064179 G A upstream_gene_variant MODIFIER c.-1646C>T| S94
40802 BAA01g25780 A01 14064293 C T upstream_gene_variant MODIFIER c.-1760G>A| S142
40803 BAA01g25780 A01 14065441 C T upstream_gene_variant MODIFIER c.-2908G>A| S192
40804 BAA01g25780 A01 14065563 C T upstream_gene_variant MODIFIER c.-3030G>A| S42
40805 BAA01g25780 A01 14067012 G A upstream_gene_variant MODIFIER c.-4479C>T| S263
40806 BAA01g25780 A01 14067128 G A upstream_gene_variant MODIFIER c.-4595C>T| S306
S308
40807 BAA01g25790 A01 14068388 C T stop_gained HIGH c.586C>T|p.Gln196* S208
S93
40808 BAA01g25790 A01 14069853 G A intron_variant MODIFIER c.1082-573G>A| S292
40809 BAA01g25790 A01 14069876 G A intron_variant MODIFIER c.1082-550G>A| S175
40810 BAA01g25790 A01 14070443 G A missense_variant MODERATE c.1099G>A|p.Gly367Arg S84
S93
40811 BAA01g25790 A01 14070630 G A missense_variant MODERATE c.1286G>A|p.Arg429Lys S59
40812 BAA01g25790 A01 14070834 G A missense_variant MODERATE c.1490G>A|p.Gly497Asp S57
40813 BAA01g25790 A01 14071589 C T downstream_gene_variant MODIFIER c.*691C>T| S289
S290
40814 BAA01g25790 A01 14071629 G A downstream_gene_variant MODIFIER c.*731G>A| S40
S49
40815 BAA01g25790 A01 14072613 C T downstream_gene_variant MODIFIER c.*1715C>T| S176
40816 BAA01g25790 A01 14072645 G A downstream_gene_variant MODIFIER c.*1747G>A| S257
40817 BAA01g25790 A01 14073195 C T downstream_gene_variant MODIFIER c.*2297C>T| S155
S211
40818 BAA01g25790 A01 14073331 C T downstream_gene_variant MODIFIER c.*2433C>T| S95
40819 BAA01g25790 A01 14074176 G A downstream_gene_variant MODIFIER c.*3278G>A| S159
S243
40820 BAA01g25790 A01 14074312 T A downstream_gene_variant MODIFIER c.*3414T>A| S139
40821 BAA01g25790 A01 14074463 G A downstream_gene_variant MODIFIER c.*3565G>A| S59
40822 BAA01g25790 A01 14074908 G A downstream_gene_variant MODIFIER c.*4010G>A| S32
40823 BAA01g25790 A01 14075418 C T downstream_gene_variant MODIFIER c.*4520C>T| S183
40824 BAA01g25790-BAA01g25800 A01 14076648 C T intergenic_region MODIFIER n.14076648C>T| S25
S264
40825 BAA01g25790-BAA01g25800 A01 14076662 C T intergenic_region MODIFIER n.14076662C>T| S81
S85