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
184151 BAA02g22410 A02 12127569 G A upstream_gene_variant MODIFIER c.-4327C>T| S10
184152 BAA02g22450 A02 12127956 C T missense_variant MODERATE c.191C>T|p.Ser64Leu S139
184153 BAA02g22450 A02 12128826 G A missense_variant MODERATE c.1061G>A|p.Arg354Lys S122
184154 BAA02g22450 A02 12129245 C T missense_variant MODERATE c.1366C>T|p.Leu456Phe S130
184155 BAA02g22430 A02 12129944 C T downstream_gene_variant MODIFIER c.*3777C>T| S84
S93
184156 BAA02g22440 A02 12131187 C T downstream_gene_variant MODIFIER c.*4359C>T| S301
S304
184157 BAA02g22450 A02 12131914 G A downstream_gene_variant MODIFIER c.*2640G>A| S298
S35
184158 BAA02g22450 A02 12132772 C T downstream_gene_variant MODIFIER c.*3498C>T| S233
184159 BAA02g22450 A02 12133283 C T downstream_gene_variant MODIFIER c.*4009C>T| S212
184160 BAA02g22450 A02 12133824 G A downstream_gene_variant MODIFIER c.*4550G>A| S169
184161 BAA02g22450 A02 12134014 G A downstream_gene_variant MODIFIER c.*4740G>A| S79
184162 BAA02g22450 A02 12134265 G A downstream_gene_variant MODIFIER c.*4991G>A| S61
184163 BAA02g22460 A02 12136571 C T intron_variant MODIFIER c.756+22G>A| S123
184164 BAA02g22460 A02 12137153 C T missense_variant MODERATE c.196G>A|p.Gly66Arg S25
184165 BAA02g22460 A02 12137817 G A upstream_gene_variant MODIFIER c.-347C>T| S287
184166 BAA02g22460 A02 12140193 G A upstream_gene_variant MODIFIER c.-2723C>T| S136
184167 BAA02g22460 A02 12140324 C T upstream_gene_variant MODIFIER c.-2854G>A| S6
184168 BAA02g22460 A02 12141571 G A upstream_gene_variant MODIFIER c.-4101C>T| S288
184169 BAA02g22460 A02 12142460 C T upstream_gene_variant MODIFIER c.-4990G>A| S234
184170 BAA02g22470 A02 12144355 C T upstream_gene_variant MODIFIER c.-4767C>T| S182
184171 BAA02g22470 A02 12144863 G A upstream_gene_variant MODIFIER c.-4259G>A| S126
184172 BAA02g22470 A02 12145376 C T upstream_gene_variant MODIFIER c.-3746C>T| S268
184173 BAA02g22470 A02 12147476 C T upstream_gene_variant MODIFIER c.-1646C>T| S182
184174 BAA02g22470 A02 12148321 G A upstream_gene_variant MODIFIER c.-801G>A| S95
184175 BAA02g22470 A02 12149834 C T missense_variant MODERATE c.356C>T|p.Thr119Ile S233