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
181051 BAA02g20710 A02 10992810 C T downstream_gene_variant MODIFIER c.*4879C>T| S87
181052 BAA02g20720 A02 10993317 C T upstream_gene_variant MODIFIER c.-4599C>T| S79
S84
181053 BAA02g20720 A02 10993441 C T upstream_gene_variant MODIFIER c.-4475C>T| S242
181054 BAA02g20720 A02 10993776 G A upstream_gene_variant MODIFIER c.-4140G>A| S295
181055 BAA02g20720 A02 10993929 A G upstream_gene_variant MODIFIER c.-3987A>G| S40
S49
181056 BAA02g20720 A02 10994371 G A upstream_gene_variant MODIFIER c.-3545G>A| S188
181057 BAA02g20720 A02 10994582 C T upstream_gene_variant MODIFIER c.-3334C>T| S293
181058 BAA02g20720 A02 10994586 T A upstream_gene_variant MODIFIER c.-3330T>A| S270
181059 BAA02g20720 A02 10994829 C T upstream_gene_variant MODIFIER c.-3087C>T| S209
181060 BAA02g20720 A02 10995158 G A upstream_gene_variant MODIFIER c.-2758G>A| S13
181061 BAA02g20720 A02 10995358 C A upstream_gene_variant MODIFIER c.-2558C>A| S275
181062 BAA02g20720 A02 10995753 C T upstream_gene_variant MODIFIER c.-2163C>T| S38
181063 BAA02g20720 A02 10995816 C T upstream_gene_variant MODIFIER c.-2100C>T| S207
181064 BAA02g20720 A02 10995851 C T upstream_gene_variant MODIFIER c.-2065C>T| S181
181065 BAA02g20720 A02 10996600 C T upstream_gene_variant MODIFIER c.-1316C>T| S8
181066 BAA02g20720 A02 10997851 C T upstream_gene_variant MODIFIER c.-65C>T| S8
181067 BAA02g20720 A02 10997974 G A missense_variant MODERATE c.59G>A|p.Gly20Asp S45
181068 BAA02g20720 A02 10998347 C T missense_variant MODERATE c.278C>T|p.Pro93Leu S56
181069 BAA02g20720 A02 10998633 C T splice_region_variant&intron_variant LOW c.472+8C>T| S135
181070 BAA02g20720 A02 10998924 G A missense_variant MODERATE c.692G>A|p.Arg231His S110
181071 BAA02g20720 A02 10999803 G A synonymous_variant LOW c.1254G>A|p.Lys418Lys S62
181072 BAA02g20720 A02 11000941 C T downstream_gene_variant MODIFIER c.*1117C>T| S178
181073 BAA02g20720 A02 11001207 G A downstream_gene_variant MODIFIER c.*1383G>A| S136
181074 BAA02g20720 A02 11001404 C T downstream_gene_variant MODIFIER c.*1580C>T| S212
181075 BAA02g20720 A02 11002796 G A downstream_gene_variant MODIFIER c.*2972G>A| S295