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
182301 BAA02g21360 A02 11449743 G A synonymous_variant LOW c.582C>T|p.Ser194Ser S150
182302 BAA02g21360 A02 11450195 C T missense_variant MODERATE c.130G>A|p.Val44Ile S99
182303 BAA02g21360 A02 11451004 G A upstream_gene_variant MODIFIER c.-680C>T| S116
182304 BAA02g21360 A02 11451305 G A upstream_gene_variant MODIFIER c.-981C>T| S202
182305 BAA02g21360 A02 11452020 G A upstream_gene_variant MODIFIER c.-1696C>T| S159
S243
182306 BAA02g21360 A02 11453152 G A upstream_gene_variant MODIFIER c.-2828C>T| S68
182307 BAA02g21360 A02 11453420 C T upstream_gene_variant MODIFIER c.-3096G>A| S301
S304
182308 BAA02g21370 A02 11453828 G A missense_variant MODERATE c.44G>A|p.Arg15Lys S187
182309 BAA02g21370 A02 11453985 G A stop_gained HIGH c.201G>A|p.Trp67* S197
182310 BAA02g21370 A02 11454061 C T missense_variant MODERATE c.277C>T|p.Leu93Phe S245
182311 BAA02g21380 A02 11455355 G A downstream_gene_variant MODIFIER c.*3433C>T| S197
182312 BAA02g21370 A02 11455964 C T downstream_gene_variant MODIFIER c.*391C>T| S42
182313 BAA02g21370 A02 11455965 C T downstream_gene_variant MODIFIER c.*392C>T| S273
182314 BAA02g21380 A02 11460566 C T upstream_gene_variant MODIFIER c.-791G>A| S159
S188
S243
S276
S298
S299
182315 BAA02g21380 A02 11460775 C T upstream_gene_variant MODIFIER c.-1000G>A| S255
182316 BAA02g21380 A02 11462420 G A upstream_gene_variant MODIFIER c.-2645C>T| S133
182317 BAA02g21380 A02 11462983 C T upstream_gene_variant MODIFIER c.-3208G>A| S183
S198
182318 BAA02g21380-BAA02g21390 A02 11464955 G A intergenic_region MODIFIER n.11464955G>A| S35
182319 BAA02g21380-BAA02g21390 A02 11465634 C T intergenic_region MODIFIER n.11465634C>T| S108
182320 BAA02g21380-BAA02g21390 A02 11465882 C T intergenic_region MODIFIER n.11465882C>T| S165
182321 BAA02g21380-BAA02g21390 A02 11466354 C T intergenic_region MODIFIER n.11466354C>T| S301
S304
182322 BAA02g21380-BAA02g21390 A02 11467129 C T intergenic_region MODIFIER n.11467129C>T| S100
182323 BAA02g21380-BAA02g21390 A02 11467480 G A intergenic_region MODIFIER n.11467480G>A| S129
182324 BAA02g21380-BAA02g21390 A02 11468843 G A intergenic_region MODIFIER n.11468843G>A| S48
182325 BAA02g21380-BAA02g21390 A02 11468879 C T intergenic_region MODIFIER n.11468879C>T| S2
S4
S6