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
197051 BAA02g29110 A02 16600484 A C missense_variant MODERATE c.677A>C|p.Gln226Pro S146
197052 BAA02g29110 A02 16600652 C T missense_variant MODERATE c.770C>T|p.Pro257Leu S42
197053 BAA02g29100 A02 16601213 G A upstream_gene_variant MODIFIER c.-3189C>T| S205
197054 BAA02g29100 A02 16601227 G A upstream_gene_variant MODIFIER c.-3203C>T| S122
197055 BAA02g29110 A02 16602245 C T stop_gained HIGH c.1432C>T|p.Gln478* S171
197056 BAA02g29110 A02 16604206 C T downstream_gene_variant MODIFIER c.*19C>T| S78
S83
197057 BAA02g29110 A02 16604531 G A downstream_gene_variant MODIFIER c.*344G>A| S129
197058 BAA02g29110 A02 16605327 G A downstream_gene_variant MODIFIER c.*1140G>A| S33
197059 BAA02g29110 A02 16606007 G A downstream_gene_variant MODIFIER c.*1820G>A| S247
197060 BAA02g29110 A02 16606227 C T downstream_gene_variant MODIFIER c.*2040C>T| S138
197061 BAA02g29120 A02 16607398 G A upstream_gene_variant MODIFIER c.-341C>T| S294
197062 BAA02g29120 A02 16607798 C T upstream_gene_variant MODIFIER c.-741G>A| S40
S49
197063 BAA02g29120 A02 16608142 C T upstream_gene_variant MODIFIER c.-1085G>A| S40
S49
197064 BAA02g29120 A02 16608176 C T upstream_gene_variant MODIFIER c.-1119G>A| S176
197065 BAA02g29120 A02 16609210 C T upstream_gene_variant MODIFIER c.-2153G>A| S157
S163
197066 BAA02g29120 A02 16609572 G A upstream_gene_variant MODIFIER c.-2515C>T| S25
197067 BAA02g29120 A02 16610051 G A upstream_gene_variant MODIFIER c.-2994C>T| S13
S140
S168
S279
197068 BAA02g29120 A02 16610247 C T upstream_gene_variant MODIFIER c.-3190G>A| S289
S290
197069 BAA02g29120 A02 16610268 G A upstream_gene_variant MODIFIER c.-3211C>T| S36
197070 BAA02g29120 A02 16611310 G A upstream_gene_variant MODIFIER c.-4253C>T| S34
197071 BAA02g29120 A02 16611681 T A upstream_gene_variant MODIFIER c.-4624A>T| S246
197072 BAA02g29120-BAA02g29130 A02 16613602 C T intergenic_region MODIFIER n.16613602C>T| S107
197073 BAA02g29120-BAA02g29130 A02 16613913 C T intergenic_region MODIFIER n.16613913C>T| S216
197074 BAA02g29120-BAA02g29130 A02 16614171 C T intergenic_region MODIFIER n.16614171C>T| S231
197075 BAA02g29120-BAA02g29130 A02 16615774 C T intergenic_region MODIFIER n.16615774C>T| S100