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
171151 BAA02g15480 A02 7475257 C T upstream_gene_variant MODIFIER c.-2017C>T| S15
S2
S3
S34
S4
S6
171152 BAA02g15480 A02 7475290 G A upstream_gene_variant MODIFIER c.-1984G>A| S153
S213
171153 BAA02g15480 A02 7475686 G A upstream_gene_variant MODIFIER c.-1588G>A| S217
S248
171154 BAA02g15480 A02 7477041 C T upstream_gene_variant MODIFIER c.-233C>T| S47
171155 BAA02g15480 A02 7477179 C T upstream_gene_variant MODIFIER c.-95C>T| S167
171156 BAA02g15480 A02 7477710 G A missense_variant MODERATE c.437G>A|p.Gly146Asp S210
171157 BAA02g15480 A02 7478402 C T downstream_gene_variant MODIFIER c.*487C>T| S275
171158 BAA02g15490 A02 7478673 G A splice_region_variant&intron_variant LOW c.324-3C>T| S264
171159 BAA02g15480 A02 7478910 G A downstream_gene_variant MODIFIER c.*995G>A| S95
171160 BAA02g15490 A02 7479013 C T synonymous_variant LOW c.210G>A|p.Pro70Pro S183
S198
171161 BAA02g15490 A02 7479703 A C upstream_gene_variant MODIFIER c.-395T>G| S250
171162 BAA02g15500 A02 7480097 G A missense_variant MODERATE c.869C>T|p.Thr290Ile S172
S217
171163 BAA02g15500 A02 7480553 C T missense_variant MODERATE c.413G>A|p.Gly138Asp S6
171164 BAA02g15490 A02 7481195 G A upstream_gene_variant MODIFIER c.-1887C>T| S170
171165 BAA02g15490 A02 7481465 G A upstream_gene_variant MODIFIER c.-2157C>T| S296
171166 BAA02g15490 A02 7481538 G A upstream_gene_variant MODIFIER c.-2230C>T| S113
171167 BAA02g15490 A02 7481686 C T upstream_gene_variant MODIFIER c.-2378G>A| S273
171168 BAA02g15490 A02 7483563 G A upstream_gene_variant MODIFIER c.-4255C>T| S223
171169 BAA02g15490 A02 7483849 G A upstream_gene_variant MODIFIER c.-4541C>T| S61
171170 BAA02g15500 A02 7484529 C T upstream_gene_variant MODIFIER c.-3478G>A| S284
171171 BAA02g15500 A02 7485246 C T upstream_gene_variant MODIFIER c.-4195G>A| S267
171172 BAA02g15500 A02 7485529 G A upstream_gene_variant MODIFIER c.-4478C>T| S231
171173 BAA02g15500 A02 7485666 C T upstream_gene_variant MODIFIER c.-4615G>A| S180
171174 BAA02g15500 A02 7485917 G A upstream_gene_variant MODIFIER c.-4866C>T| S190
171175 BAA02g15510 A02 7487496 G A upstream_gene_variant MODIFIER c.-1069C>T| S166