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
106051 BAA10g08190 A10 5846612 G A upstream_gene_variant MODIFIER c.-1594G>A| S187
106052 BAA10g08190 A10 5847957 G A upstream_gene_variant MODIFIER c.-249G>A| S15
106053 BAA10g08190 A10 5849052 G A intron_variant MODIFIER c.172-45G>A| S127
106054 BAA10g08190 A10 5849093 C T splice_region_variant&intron_variant LOW c.172-4C>T| S194
106055 BAA10g08190 A10 5849318 C T synonymous_variant LOW c.393C>T|p.Leu131Leu S152
106056 BAA10g08190 A10 5849698 G A missense_variant MODERATE c.706G>A|p.Glu236Lys S99
106057 BAA10g08190 A10 5850186 G A downstream_gene_variant MODIFIER c.*321G>A| S69
106058 BAA10g08190 A10 5850389 C T downstream_gene_variant MODIFIER c.*524C>T| S131
106059 BAA10g08190 A10 5850837 C T downstream_gene_variant MODIFIER c.*972C>T| S281
106060 BAA10g08190 A10 5851129 C T downstream_gene_variant MODIFIER c.*1264C>T| S296
106061 BAA10g08190 A10 5852198 C T downstream_gene_variant MODIFIER c.*2333C>T| S84
S93
106062 BAA10g08190 A10 5852408 G A downstream_gene_variant MODIFIER c.*2543G>A| S278
106063 BAA10g08190 A10 5852504 G A downstream_gene_variant MODIFIER c.*2639G>A| S140
106064 BAA10g08190 A10 5852736 C T downstream_gene_variant MODIFIER c.*2871C>T| S37
106065 BAA10g08190 A10 5853315 G A downstream_gene_variant MODIFIER c.*3450G>A| S17
106066 BAA10g08190 A10 5853586 C T downstream_gene_variant MODIFIER c.*3721C>T| S199
106067 BAA10g08190 A10 5853811 G A downstream_gene_variant MODIFIER c.*3946G>A| S43
106068 BAA10g08190 A10 5854028 G A downstream_gene_variant MODIFIER c.*4163G>A| S55
106069 BAA10g08190 A10 5854136 G A downstream_gene_variant MODIFIER c.*4271G>A| S234
106070 BAA10g08190 A10 5854175 G A downstream_gene_variant MODIFIER c.*4310G>A| S237
106071 BAA10g08190 A10 5854338 C T downstream_gene_variant MODIFIER c.*4473C>T| S38
106072 BAA10g08190 A10 5854342 G A downstream_gene_variant MODIFIER c.*4477G>A| S250
106073 BAA10g08190 A10 5854359 G A downstream_gene_variant MODIFIER c.*4494G>A| S18
106074 BAA10g08190 A10 5854645 C T downstream_gene_variant MODIFIER c.*4780C>T| S142
106075 BAA10g08190-BAA10g08200 A10 5855460 G A intergenic_region MODIFIER n.5855460G>A| S296