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
197151 BAA02g29120-BAA02g29130 A02 16627885 C T intergenic_region MODIFIER n.16627885C>T| S120
197152 BAA02g29120-BAA02g29130 A02 16627944 C T intergenic_region MODIFIER n.16627944C>T| S268
197153 BAA02g29130 A02 16630457 C T downstream_gene_variant MODIFIER c.*4713G>A| S54
197154 BAA02g29130 A02 16630950 C T downstream_gene_variant MODIFIER c.*4220G>A| S171
197155 BAA02g29130 A02 16631144 G A downstream_gene_variant MODIFIER c.*4026C>T| S187
197156 BAA02g29130 A02 16632557 G A downstream_gene_variant MODIFIER c.*2613C>T| S10
197157 BAA02g29130 A02 16633371 C T downstream_gene_variant MODIFIER c.*1799G>A| S161
197158 BAA02g29130 A02 16634038 C T downstream_gene_variant MODIFIER c.*1132G>A| S32
197159 BAA02g29130 A02 16635731 G A synonymous_variant LOW c.1108C>T|p.Leu370Leu S153
S213
197160 BAA02g29130 A02 16636749 G A missense_variant MODERATE c.653C>T|p.Ser218Phe S272
197161 BAA02g29130 A02 16637482 G A synonymous_variant LOW c.243C>T|p.Asp81Asp S153
S213
197162 BAA02g29130 A02 16637552 G A missense_variant MODERATE c.173C>T|p.Ser58Phe S17
197163 BAA02g29130 A02 16637652 G A missense_variant MODERATE c.73C>T|p.Leu25Phe S209
197164 BAA02g29130 A02 16638349 G A upstream_gene_variant MODIFIER c.-625C>T| S148
S210
S30
S31
197165 BAA02g29200-BAA02g29210 A02 16682750 G A intergenic_region MODIFIER n.16682750G>A| S139
197166 BAA02g29210 A02 16690835 C T upstream_gene_variant MODIFIER c.-949C>T| S249
197167 BAA02g29210 A02 16692642 C T missense_variant MODERATE c.859C>T|p.Leu287Phe S18
197168 BAA02g29220 A02 16695316 G A missense_variant MODERATE c.353G>A|p.Gly118Glu S298
197169 BAA02g29210 A02 16695878 C T downstream_gene_variant MODIFIER c.*1704C>T| S18
197170 BAA02g29210 A02 16696766 G A downstream_gene_variant MODIFIER c.*2592G>A| S247
197171 BAA02g29210 A02 16697304 G A downstream_gene_variant MODIFIER c.*3130G>A| S136
197172 BAA02g29210 A02 16697443 G A downstream_gene_variant MODIFIER c.*3269G>A| S223
197173 BAA02g29210 A02 16697865 C T downstream_gene_variant MODIFIER c.*3691C>T| S301
S304
197174 BAA02g29210 A02 16697869 C T downstream_gene_variant MODIFIER c.*3695C>T| S105
S106
197175 BAA02g29210 A02 16698546 G A downstream_gene_variant MODIFIER c.*4372G>A| S278