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
165851 BAA02g12020 A02 5424169 G A upstream_gene_variant MODIFIER c.-864C>T| S164
165852 BAA02g12020 A02 5424766 C T upstream_gene_variant MODIFIER c.-1461G>A| S221
S258
165853 BAA02g12020 A02 5427423 G A upstream_gene_variant MODIFIER c.-4118C>T| S223
165854 BAA02g12020 A02 5428128 C T upstream_gene_variant MODIFIER c.-4823G>A| S186
165855 BAA02g12030 A02 5428503 G A downstream_gene_variant MODIFIER c.*182C>T| S53
S75
S81
S82
S92
165856 BAA02g12030 A02 5428627 G A downstream_gene_variant MODIFIER c.*58C>T| S256
165857 BAA02g12030 A02 5429037 G A missense_variant MODERATE c.1853C>T|p.Ala618Val S197
165858 BAA02g12030 A02 5429139 G A missense_variant MODERATE c.1751C>T|p.Thr584Ile S274
165859 BAA02g12030 A02 5430793 C T missense_variant MODERATE c.662G>A|p.Gly221Glu S211
S227
165860 BAA02g12030 A02 5430797 G A missense_variant MODERATE c.658C>T|p.Leu220Phe S246
165861 BAA02g12030 A02 5431160 G A synonymous_variant LOW c.393C>T|p.Asn131Asn S269
165862 BAA02g12030 A02 5431228 G A synonymous_variant LOW c.325C>T|p.Leu109Leu S57
165863 BAA02g12030 A02 5431640 G A missense_variant MODERATE c.148C>T|p.Pro50Ser S228
165864 BAA02g12030 A02 5433141 C T upstream_gene_variant MODIFIER c.-1245G>A| S66
165865 BAA02g12030 A02 5433497 G A upstream_gene_variant MODIFIER c.-1601C>T| S289
S290
165866 BAA02g12030 A02 5433830 G A upstream_gene_variant MODIFIER c.-1934C>T| S190
165867 BAA02g12030 A02 5434638 C T upstream_gene_variant MODIFIER c.-2742G>A| S135
165868 BAA02g12030 A02 5434726 C T upstream_gene_variant MODIFIER c.-2830G>A| S104
165869 BAA02g12030 A02 5435091 G A upstream_gene_variant MODIFIER c.-3195C>T| S197
165870 BAA02g12040 A02 5437221 G A upstream_gene_variant MODIFIER c.-5G>A| S203
165871 BAA02g12050 A02 5437528 G A upstream_gene_variant MODIFIER c.-3050G>A| S20
165872 BAA02g12050 A02 5437927 C T upstream_gene_variant MODIFIER c.-2651C>T| S275
165873 BAA02g12040 A02 5438384 C T missense_variant MODERATE c.284C>T|p.Thr95Ile S272
165874 BAA02g12040 A02 5438594 C T missense_variant MODERATE c.494C>T|p.Ser165Leu S186
165875 BAA02g12050 A02 5439227 G A upstream_gene_variant MODIFIER c.-1351G>A| S159
S243