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
200251 BAA02g30390 A02 17736881 C T upstream_gene_variant MODIFIER c.-1376G>A| S206
200252 BAA02g30390 A02 17737014 G A upstream_gene_variant MODIFIER c.-1509C>T| S256
200253 BAA02g30390 A02 17737920 G A upstream_gene_variant MODIFIER c.-2415C>T| S19
200254 BAA02g30390 A02 17737983 G A upstream_gene_variant MODIFIER c.-2478C>T| S286
200255 BAA02g30390 A02 17738930 C T upstream_gene_variant MODIFIER c.-3425G>A| S172
200256 BAA02g30390 A02 17739189 C T upstream_gene_variant MODIFIER c.-3684G>A| S112
200257 BAA02g30390 A02 17739253 C T upstream_gene_variant MODIFIER c.-3748G>A| S299
200258 BAA02g30390 A02 17740188 C T upstream_gene_variant MODIFIER c.-4683G>A| S142
200259 BAA02g30400 A02 17741662 C T upstream_gene_variant MODIFIER c.-1869C>T| S139
200260 BAA02g30400 A02 17742171 C T upstream_gene_variant MODIFIER c.-1360C>T| S218
200261 BAA02g30400 A02 17743143 C T upstream_gene_variant MODIFIER c.-388C>T| S64
200262 BAA02g30400 A02 17743560 G A stop_gained HIGH c.30G>A|p.Trp10* S269
200263 BAA02g30400 A02 17744137 G C missense_variant&splice_region_variant MODERATE c.425G>C|p.Ser142Thr S176
200264 BAA02g30400 A02 17745362 C T intron_variant MODIFIER c.888-21C>T| S130
200265 BAA02g30400 A02 17745786 C T missense_variant MODERATE c.1291C>T|p.Pro431Ser S177
200266 BAA02g30400 A02 17745817 C T missense_variant MODERATE c.1322C>T|p.Ala441Val S2
200267 BAA02g30400 A02 17745829 G A missense_variant MODERATE c.1334G>A|p.Arg445Lys S111
200268 BAA02g30400 A02 17746189 C T downstream_gene_variant MODIFIER c.*248C>T| S65
200269 BAA02g30400 A02 17747239 G A downstream_gene_variant MODIFIER c.*1298G>A| S55
200270 BAA02g30400 A02 17747551 C T downstream_gene_variant MODIFIER c.*1610C>T| S92
200271 BAA02g30400 A02 17748892 G A downstream_gene_variant MODIFIER c.*2951G>A| S298
200272 BAA02g30400 A02 17748900 C T downstream_gene_variant MODIFIER c.*2959C>T| S246
200273 BAA02g30400 A02 17749107 C T downstream_gene_variant MODIFIER c.*3166C>T| S66
200274 BAA02g30400 A02 17749721 C T downstream_gene_variant MODIFIER c.*3780C>T| S100
200275 BAA02g30400 A02 17750483 G A downstream_gene_variant MODIFIER c.*4542G>A| S12