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
151151 BAA02g00020 A02 15110 G A upstream_gene_variant MODIFIER c.-2658G>A| S81
S85
151152 BAA02g00020 A02 15208 C T upstream_gene_variant MODIFIER c.-2560C>T| S277
151153 BAA02g00020 A02 16839 C T upstream_gene_variant MODIFIER c.-929C>T| S159
151154 BAA02g00020 A02 16878 C T upstream_gene_variant MODIFIER c.-890C>T| S194
151155 BAA02g00020 A02 16896 G A upstream_gene_variant MODIFIER c.-872G>A| S153
151156 BAA02g00020 A02 17109 T A upstream_gene_variant MODIFIER c.-659T>A| S94
151157 BAA02g00020 A02 17761 C T upstream_gene_variant MODIFIER c.-7C>T| S139
151158 BAA02g00020 A02 18662 G A missense_variant MODERATE c.714G>A|p.Met238Ile S295
151159 BAA02g00030 A02 19147 G A upstream_gene_variant MODIFIER c.-2578G>A| S295
151160 BAA02g00030 A02 19434 G A upstream_gene_variant MODIFIER c.-2291G>A| S25
151161 BAA02g00030 A02 19976 C T upstream_gene_variant MODIFIER c.-1749C>T| S274
151162 BAA02g00030 A02 20352 C T upstream_gene_variant MODIFIER c.-1373C>T| S66
151163 BAA02g00030 A02 20368 C T upstream_gene_variant MODIFIER c.-1357C>T| S274
151164 BAA02g00030 A02 20826 G A upstream_gene_variant MODIFIER c.-899G>A| S155
S211
151165 BAA02g00030 A02 22241 G A missense_variant MODERATE c.517G>A|p.Val173Ile S139
151166 BAA02g00030 A02 22817 C T missense_variant MODERATE c.1093C>T|p.Pro365Ser S277
151167 BAA02g00030 A02 22952 G A missense_variant MODERATE c.1228G>A|p.Asp410Asn S148
S30
S31
151168 BAA02g00030 A02 22970 G A missense_variant MODERATE c.1246G>A|p.Glu416Lys S10
151169 BAA02g00030 A02 23574 G A synonymous_variant LOW c.1749G>A|p.Gln583Gln S232
151170 BAA02g00030 A02 24111 C T synonymous_variant LOW c.2199C>T|p.Tyr733Tyr S130
151171 BAA02g00030 A02 24461 G A missense_variant MODERATE c.2549G>A|p.Gly850Glu S244
151172 BAA02g00030 A02 24672 G A synonymous_variant LOW c.2760G>A|p.Pro920Pro S266
151173 BAA02g00030 A02 26228 G A intron_variant MODIFIER c.2814+1502G>A| S4
151174 BAA02g00030 A02 26437 G A intron_variant MODIFIER c.2814+1711G>A| S158
151175 BAA02g00030 A02 26463 G A intron_variant MODIFIER c.2814+1737G>A| S149