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
191101 BAA02g26290 A02 14588296 G A downstream_gene_variant MODIFIER c.*3224C>T| S133
191102 BAA02g26290 A02 14588403 C T downstream_gene_variant MODIFIER c.*3117G>A| S33
191103 BAA02g26290 A02 14590178 G A downstream_gene_variant MODIFIER c.*1342C>T| S129
191104 BAA02g26290 A02 14590714 C T downstream_gene_variant MODIFIER c.*806G>A| S182
191105 BAA02g26290 A02 14591057 C T downstream_gene_variant MODIFIER c.*463G>A| S42
191106 BAA02g26290 A02 14591342 G A downstream_gene_variant MODIFIER c.*178C>T| S122
191107 BAA02g26290 A02 14592661 G A missense_variant MODERATE c.1580C>T|p.Ser527Phe S236
191108 BAA02g26290 A02 14592747 G A synonymous_variant LOW c.1494C>T|p.Pro498Pro S94
191109 BAA02g26290 A02 14593470 G A synonymous_variant LOW c.1287C>T|p.Phe429Phe S127
191110 BAA02g26290 A02 14594261 G A missense_variant MODERATE c.643C>T|p.Leu215Phe S204
191111 BAA02g26290 A02 14595051 G A synonymous_variant LOW c.171C>T|p.Asp57Asp S156
191112 BAA02g26290 A02 14595523 C T upstream_gene_variant MODIFIER c.-302G>A| S296
191113 BAA02g26290 A02 14595880 G A upstream_gene_variant MODIFIER c.-659C>T| S143
191114 BAA02g26290 A02 14597684 C T upstream_gene_variant MODIFIER c.-2463G>A| S32
191115 BAA02g26290 A02 14599213 C T upstream_gene_variant MODIFIER c.-3992G>A| S33
191116 BAA02g26300 A02 14600914 G A upstream_gene_variant MODIFIER c.-3998G>A| S72
S78
191117 BAA02g26300 A02 14601417 G A upstream_gene_variant MODIFIER c.-3495G>A| S251
191118 BAA02g26300 A02 14601909 C T upstream_gene_variant MODIFIER c.-3003C>T| S118
191119 BAA02g26300 A02 14603493 C T upstream_gene_variant MODIFIER c.-1419C>T| S176
191120 BAA02g26300 A02 14604102 G A upstream_gene_variant MODIFIER c.-810G>A| S210
S225
191121 BAA02g26300 A02 14604220 G A upstream_gene_variant MODIFIER c.-692G>A| S298
191122 BAA02g26300 A02 14605015 G A missense_variant MODERATE c.104G>A|p.Arg35Lys S70
191123 BAA02g26300 A02 14605499 G A splice_acceptor_variant&intron_variant HIGH c.268-1G>A| S184
191124 BAA02g26300 A02 14606066 G A downstream_gene_variant MODIFIER c.*246G>A| S269
191125 BAA02g26310 A02 14606198 C T missense_variant MODERATE c.761G>A|p.Arg254Lys S138