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
15251 BAA01g11750 A01 5464700 G A upstream_gene_variant MODIFIER c.-58C>T| S276
15252 BAA01g11750 A01 5465256 G A upstream_gene_variant MODIFIER c.-614C>T| S34
15253 BAA01g11760 A01 5473740 G A intron_variant MODIFIER c.337-23C>T| S183
S198
15254 BAA01g11760 A01 5473843 G A intron_variant MODIFIER c.336+41C>T| S121
15255 BAA01g11760 A01 5474496 G A missense_variant MODERATE c.10C>T|p.Pro4Ser S154
S95
15256 BAA01g11760 A01 5474519 G A upstream_gene_variant MODIFIER c.-14C>T| S72
15257 BAA01g11760 A01 5474657 C T upstream_gene_variant MODIFIER c.-152G>A| S266
15258 BAA01g11760 A01 5474667 G A upstream_gene_variant MODIFIER c.-162C>T| S86
15259 BAA01g11760 A01 5475104 C T upstream_gene_variant MODIFIER c.-599G>A| S244
15260 BAA01g11760 A01 5475766 G T upstream_gene_variant MODIFIER c.-1261C>A| S268
15261 BAA01g11760 A01 5475783 C T upstream_gene_variant MODIFIER c.-1278G>A| S40
S49
15262 BAA01g11760 A01 5477127 G A upstream_gene_variant MODIFIER c.-2622C>T| S199
15263 BAA01g11760 A01 5477206 C T upstream_gene_variant MODIFIER c.-2701G>A| S48
15264 BAA01g11760 A01 5477359 G A upstream_gene_variant MODIFIER c.-2854C>T| S45
15265 BAA01g11760 A01 5477547 G A upstream_gene_variant MODIFIER c.-3042C>T| S70
15266 BAA01g11760 A01 5477572 G A upstream_gene_variant MODIFIER c.-3067C>T| S187
15267 BAA01g11760 A01 5477787 C T upstream_gene_variant MODIFIER c.-3282G>A| S6
15268 BAA01g11760 A01 5479069 G A upstream_gene_variant MODIFIER c.-4564C>T| S59
15269 BAA01g11770 A01 5480013 G A upstream_gene_variant MODIFIER c.-1331G>A| S56
15270 BAA01g11770 A01 5480063 G A upstream_gene_variant MODIFIER c.-1281G>A| S208
S219
15271 BAA01g11770 A01 5480852 C T upstream_gene_variant MODIFIER c.-492C>T| S299
15272 BAA01g11770 A01 5481249 C T upstream_gene_variant MODIFIER c.-95C>T| S265
15273 BAA01g11770 A01 5482570 C T downstream_gene_variant MODIFIER c.*1026C>T| S77
S82
15274 BAA01g11770 A01 5482728 C T downstream_gene_variant MODIFIER c.*1184C>T| S286
15275 BAA01g11780 A01 5483523 G A missense_variant MODERATE c.229C>T|p.Leu77Phe S59