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
175951 BAA02g18130-BAA02g18140 A02 9126548 C T intergenic_region MODIFIER n.9126548C>T| S163
175952 BAA02g18130-BAA02g18140 A02 9127697 A T intergenic_region MODIFIER n.9127697A>T| S136
175953 BAA02g18130-BAA02g18140 A02 9129776 C T intergenic_region MODIFIER n.9129776C>T| S182
175954 BAA02g18130-BAA02g18140 A02 9130157 G A intergenic_region MODIFIER n.9130157G>A| S306
S308
175955 BAA02g18130-BAA02g18140 A02 9131161 G A intergenic_region MODIFIER n.9131161G>A| S159
S243
175956 BAA02g18130-BAA02g18140 A02 9132244 C T intergenic_region MODIFIER n.9132244C>T| S34
175957 BAA02g18130-BAA02g18140 A02 9132252 C T intergenic_region MODIFIER n.9132252C>T| S260
175958 BAA02g18140 A02 9133363 C T upstream_gene_variant MODIFIER c.-4311C>T| S308
175959 BAA02g18140 A02 9133730 C T upstream_gene_variant MODIFIER c.-3944C>T| S209
175960 BAA02g18140 A02 9134970 C T upstream_gene_variant MODIFIER c.-2704C>T| S105
S106
175961 BAA02g18140 A02 9135095 G A upstream_gene_variant MODIFIER c.-2579G>A| S293
175962 BAA02g18140 A02 9137738 C T missense_variant MODERATE c.65C>T|p.Ser22Phe S171
175963 BAA02g18140 A02 9137959 G A intron_variant MODIFIER c.82+204G>A| S10
175964 BAA02g18140 A02 9138483 G A synonymous_variant LOW c.264G>A|p.Gln88Gln S17
175965 BAA02g18140 A02 9138801 G A synonymous_variant LOW c.582G>A|p.Gln194Gln S282
175966 BAA02g18140 A02 9140711 G A downstream_gene_variant MODIFIER c.*676G>A| S146
175967 BAA02g18140 A02 9140877 G A downstream_gene_variant MODIFIER c.*842G>A| S37
175968 BAA02g18140 A02 9141081 G A downstream_gene_variant MODIFIER c.*1046G>A| S82
S92
175969 BAA02g18140 A02 9141637 C T downstream_gene_variant MODIFIER c.*1602C>T| S176
175970 BAA02g18140 A02 9144809 C T downstream_gene_variant MODIFIER c.*4774C>T| S218
175971 BAA02g18150 A02 9145097 C T downstream_gene_variant MODIFIER c.*359G>A| S209
175972 BAA02g18150 A02 9146345 C T intron_variant MODIFIER c.952-311G>A| S175
175973 BAA02g18150 A02 9147273 C T missense_variant MODERATE c.491G>A|p.Cys164Tyr S299
175974 BAA02g18150 A02 9147287 C T synonymous_variant LOW c.477G>A|p.Glu159Glu S179
175975 BAA02g18150 A02 9147418 C T missense_variant MODERATE c.346G>A|p.Ala116Thr S25