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
178201 BAA02g19160 A02 9956155 G T missense_variant MODERATE c.286G>T|p.Val96Leu S153
S213
178202 BAA02g19160 A02 9956191 G A missense_variant MODERATE c.322G>A|p.Ala108Thr S297
178203 BAA02g19170 A02 9957126 C T upstream_gene_variant MODIFIER c.-89C>T| S167
178204 BAA02g19170 A02 9957493 G A synonymous_variant LOW c.279G>A|p.Glu93Glu S20
178205 BAA02g19170 A02 9957586 G A synonymous_variant LOW c.372G>A|p.Pro124Pro S282
178206 BAA02g19170 A02 9957810 G A missense_variant MODERATE c.596G>A|p.Arg199Gln S98
178207 BAA02g19180 A02 9958556 C T upstream_gene_variant MODIFIER c.-3244C>T| S163
178208 BAA02g19180 A02 9960212 C T upstream_gene_variant MODIFIER c.-1588C>T| S305
178209 BAA02g19180 A02 9960604 G A upstream_gene_variant MODIFIER c.-1196G>A| S10
178210 BAA02g19180 A02 9960717 C T upstream_gene_variant MODIFIER c.-1083C>T| S186
178211 BAA02g19180 A02 9961115 C T upstream_gene_variant MODIFIER c.-685C>T| S25
178212 BAA02g19180 A02 9961184 C T upstream_gene_variant MODIFIER c.-616C>T| S171
178213 BAA02g19170 A02 9962112 G A downstream_gene_variant MODIFIER c.*4082G>A| S126
178214 BAA02g19170 A02 9962332 C T downstream_gene_variant MODIFIER c.*4302C>T| S219
178215 BAA02g19180 A02 9962696 G A missense_variant MODERATE c.688G>A|p.Val230Ile S274
178216 BAA02g19180 A02 9963366 G A downstream_gene_variant MODIFIER c.*197G>A| S296
178217 BAA02g19180 A02 9964765 G A downstream_gene_variant MODIFIER c.*1596G>A| S256
178218 BAA02g19190 A02 9965837 G A synonymous_variant LOW c.252C>T|p.Ser84Ser S187
178219 BAA02g19190 A02 9966440 G A upstream_gene_variant MODIFIER c.-264C>T| S23
178220 BAA02g19190 A02 9966969 C T upstream_gene_variant MODIFIER c.-793G>A| S206
178221 BAA02g19190 A02 9969666 C T upstream_gene_variant MODIFIER c.-3490G>A| S183
S198
178222 BAA02g19190 A02 9970438 G A upstream_gene_variant MODIFIER c.-4262C>T| S302
178223 BAA02g19190 A02 9970540 G A upstream_gene_variant MODIFIER c.-4364C>T| S20
178224 BAA02g19190 A02 9970913 G A upstream_gene_variant MODIFIER c.-4737C>T| S187
178225 BAA02g19190 A02 9970946 C T upstream_gene_variant MODIFIER c.-4770G>A| S152