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
153701 BAA02g02100 A02 941713 G A downstream_gene_variant MODIFIER c.*2129G>A| S10
153702 BAA02g02100 A02 942088 G A downstream_gene_variant MODIFIER c.*2504G>A| S249
153703 BAA02g02100 A02 942500 G A downstream_gene_variant MODIFIER c.*2916G>A| S156
153704 BAA02g02100 A02 943919 G A downstream_gene_variant MODIFIER c.*4335G>A| S190
153705 BAA02g02110 A02 945152 C T downstream_gene_variant MODIFIER c.*1112G>A| S40
S49
153706 BAA02g02110 A02 946733 G A intron_variant MODIFIER c.409-152C>T| S162
153707 BAA02g02110 A02 948079 G A intron_variant MODIFIER c.238-780C>T| S204
153708 BAA02g02110 A02 948394 T A intron_variant MODIFIER c.238-1095A>T| S119
153709 BAA02g02110 A02 952753 C T intron_variant MODIFIER c.237+782G>A| S111
153710 BAA02g02110 A02 952779 C A intron_variant MODIFIER c.237+756G>T| S287
153711 BAA02g02110 A02 952885 G A intron_variant MODIFIER c.237+650C>T| S265
153712 BAA02g02110 A02 952933 G A intron_variant MODIFIER c.237+602C>T| S59
153713 BAA02g02120 A02 954833 G A upstream_gene_variant MODIFIER c.-4486G>A| S266
153714 BAA02g02110 A02 957094 G A upstream_gene_variant MODIFIER c.-947C>T| S48
153715 BAA02g02110 A02 957512 G A upstream_gene_variant MODIFIER c.-1365C>T| S168
153716 BAA02g02110 A02 957691 G A upstream_gene_variant MODIFIER c.-1544C>T| S174
153717 BAA02g02110 A02 958976 G A upstream_gene_variant MODIFIER c.-2829C>T| S286
153718 BAA02g02110 A02 959581 C T upstream_gene_variant MODIFIER c.-3434G>A| S71
153719 BAA02g02110 A02 959938 C T upstream_gene_variant MODIFIER c.-3791G>A| S170
153720 BAA02g02120 A02 960190 G A synonymous_variant LOW c.420G>A|p.Lys140Lys S155
153721 BAA02g02130 A02 962540 G A missense_variant MODERATE c.331G>A|p.Glu111Lys S273
153722 BAA02g02120 A02 963717 G A downstream_gene_variant MODIFIER c.*2832G>A| S68
153723 BAA02g02140 A02 965898 C T synonymous_variant LOW c.204G>A|p.Ser68Ser S135
153724 BAA02g02140 A02 966229 C T missense_variant MODERATE c.97G>A|p.Ala33Thr S104
153725 BAA02g02140 A02 966490 G A upstream_gene_variant MODIFIER c.-92C>T| S5