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
61701 BAA01g32650-BAA01g32660 A01 21606163 C T intergenic_region MODIFIER n.21606163C>T| S278
61702 BAA01g32650-BAA01g32660 A01 21606514 C T intergenic_region MODIFIER n.21606514C>T| S4
61703 BAA01g32650-BAA01g32660 A01 21607156 G A intergenic_region MODIFIER n.21607156G>A| S189
61704 BAA01g32650-BAA01g32660 A01 21607304 C T intergenic_region MODIFIER n.21607304C>T| S210
S225
61705 BAA01g32650-BAA01g32660 A01 21607437 C T intergenic_region MODIFIER n.21607437C>T| S161
S64
61706 BAA01g32650-BAA01g32660 A01 21608841 G A intergenic_region MODIFIER n.21608841G>A| S209
61707 BAA01g32650-BAA01g32660 A01 21609245 C T intergenic_region MODIFIER n.21609245C>T| S146
61708 BAA01g32650-BAA01g32660 A01 21611318 C T intergenic_region MODIFIER n.21611318C>T| S142
61709 BAA01g32650-BAA01g32660 A01 21611822 C T intergenic_region MODIFIER n.21611822C>T| S255
61710 BAA01g32650-BAA01g32660 A01 21612093 C T intergenic_region MODIFIER n.21612093C>T| S166
S167
61711 BAA01g32660 A01 21612592 G A upstream_gene_variant MODIFIER c.-4925G>A| S299
61712 BAA01g32660 A01 21613631 C T upstream_gene_variant MODIFIER c.-3886C>T| S295
61713 BAA01g32660 A01 21614865 G A upstream_gene_variant MODIFIER c.-2652G>A| S5
61714 BAA01g32660 A01 21615986 G A upstream_gene_variant MODIFIER c.-1531G>A| S38
61715 BAA01g32660 A01 21616356 C T upstream_gene_variant MODIFIER c.-1161C>T| S186
61716 BAA01g32660 A01 21617028 G A upstream_gene_variant MODIFIER c.-489G>A| S155
61717 BAA01g32660 A01 21617745 C T missense_variant MODERATE c.229C>T|p.Pro77Ser S156
61718 BAA01g32660 A01 21617800 C T missense_variant MODERATE c.284C>T|p.Ser95Phe S136
61719 BAA01g32660 A01 21617865 G A missense_variant MODERATE c.349G>A|p.Glu117Lys S122
61720 BAA01g32660 A01 21618028 G A downstream_gene_variant MODIFIER c.*95G>A| S221
61721 BAA01g32660 A01 21622787 C T downstream_gene_variant MODIFIER c.*4854C>T| S208
S93
61722 BAA01g32670 A01 21623742 C T missense_variant MODERATE c.325G>A|p.Glu109Lys S242
61723 BAA01g32670 A01 21624327 G A intron_variant MODIFIER c.316-576C>T| S138
S296
61724 BAA01g32670 A01 21625422 C T intron_variant MODIFIER c.316-1671G>A| S208
S219
61725 BAA01g32670 A01 21625594 G A intron_variant MODIFIER c.316-1843C>T| S1