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
171701 BAA02g15760 A02 7651791 C T upstream_gene_variant MODIFIER c.-694G>A| S199
171702 BAA02g15760 A02 7652014 C T upstream_gene_variant MODIFIER c.-917G>A| S276
171703 BAA02g15760 A02 7652969 T G upstream_gene_variant MODIFIER c.-1872A>C| S167
S236
S262
S263
171704 BAA02g15760 A02 7653059 G A upstream_gene_variant MODIFIER c.-1962C>T| S125
171705 BAA02g15760 A02 7653227 G A upstream_gene_variant MODIFIER c.-2130C>T| S209
171706 BAA02g15770 A02 7654031 C T synonymous_variant LOW c.186G>A|p.Lys62Lys S78
171707 BAA02g15790 A02 7655790 C T missense_variant MODERATE c.40G>A|p.Gly14Ser S206
S26
171708 BAA02g15760 A02 7656074 C T upstream_gene_variant MODIFIER c.-4977G>A| S206
S26
171709 BAA02g15760 A02 7656075 G A upstream_gene_variant MODIFIER c.-4978C>T| S298
171710 BAA02g15770 A02 7656757 G A upstream_gene_variant MODIFIER c.-2441C>T| S295
171711 BAA02g15770 A02 7657241 C T upstream_gene_variant MODIFIER c.-2925G>A| S182
171712 BAA02g15770 A02 7657479 C T upstream_gene_variant MODIFIER c.-3163G>A| S255
171713 BAA02g15770 A02 7658196 C T upstream_gene_variant MODIFIER c.-3880G>A| S159
S188
S243
S276
S298
S299
171714 BAA02g15770 A02 7658317 C T upstream_gene_variant MODIFIER c.-4001G>A| S9
171715 BAA02g15770 A02 7658917 C T upstream_gene_variant MODIFIER c.-4601G>A| S255
171716 BAA02g15790 A02 7660235 C T upstream_gene_variant MODIFIER c.-4406G>A| S104
171717 BAA02g15800 A02 7660699 C T synonymous_variant LOW c.102C>T|p.Val34Val S244
171718 BAA02g15790 A02 7660784 C T upstream_gene_variant MODIFIER c.-4955G>A| S174
S27
171719 BAA02g15790 A02 7660787 C T upstream_gene_variant MODIFIER c.-4958G>A| S233
171720 BAA02g15800 A02 7661607 C T intron_variant MODIFIER c.573+242C>T| S117
171721 BAA02g15800 A02 7661803 C T intron_variant MODIFIER c.574-361C>T| S224
171722 BAA02g15800 A02 7661813 C T intron_variant MODIFIER c.574-351C>T| S267
171723 BAA02g15800 A02 7661928 G A intron_variant MODIFIER c.574-236G>A| S289
S290
171724 BAA02g15800 A02 7662253 G A synonymous_variant LOW c.663G>A|p.Lys221Lys S19
171725 BAA02g15800 A02 7662716 C T downstream_gene_variant MODIFIER c.*199C>T| S262