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
101701 BAA10g07270 A10 4140556 A T upstream_gene_variant MODIFIER c.-2427T>A| S206
S26
101702 BAA10g07270 A10 4140709 C T upstream_gene_variant MODIFIER c.-2580G>A| S195
101703 BAA10g07270 A10 4141131 C T upstream_gene_variant MODIFIER c.-3002G>A| S19
101704 BAA10g07270 A10 4141715 G A upstream_gene_variant MODIFIER c.-3586C>T| S160
101705 BAA10g07280 A10 4142270 G A missense_variant MODERATE c.115G>A|p.Glu39Lys S157
S166
S167
S262
S290
101706 BAA10g07270 A10 4143043 G A upstream_gene_variant MODIFIER c.-4914C>T| S1
101707 BAA10g07290 A10 4143613 C T upstream_gene_variant MODIFIER c.-35C>T| S74
101708 BAA10g07300 A10 4144174 G A upstream_gene_variant MODIFIER c.-2588G>A| S33
101709 BAA10g07300 A10 4144429 C T upstream_gene_variant MODIFIER c.-2333C>T| S40
S49
101710 BAA10g07300 A10 4144508 G A upstream_gene_variant MODIFIER c.-2254G>A| S171
101711 BAA10g07300 A10 4144712 G A upstream_gene_variant MODIFIER c.-2050G>A| S211
101712 BAA10g07300 A10 4144825 G T upstream_gene_variant MODIFIER c.-1937G>T| S209
101713 BAA10g07300 A10 4145363 G A upstream_gene_variant MODIFIER c.-1399G>A| S268
101714 BAA10g07300 A10 4145495 G A upstream_gene_variant MODIFIER c.-1267G>A| S111
101715 BAA10g07300 A10 4145500 C T upstream_gene_variant MODIFIER c.-1262C>T| S87
101716 BAA10g07300 A10 4145876 C T upstream_gene_variant MODIFIER c.-886C>T| S79
S91
101717 BAA10g07300 A10 4146001 G A upstream_gene_variant MODIFIER c.-761G>A| S303
101718 BAA10g07300 A10 4146008 G A upstream_gene_variant MODIFIER c.-754G>A| S18
101719 BAA10g07300 A10 4146116 C T upstream_gene_variant MODIFIER c.-646C>T| S88
101720 BAA10g07300 A10 4146147 G A upstream_gene_variant MODIFIER c.-615G>A| S50
S51
101721 BAA10g07290 A10 4148394 G A downstream_gene_variant MODIFIER c.*4570G>A| S62
101722 BAA10g07290 A10 4148500 G A downstream_gene_variant MODIFIER c.*4676G>A| S284
101723 BAA10g07300 A10 4148953 G A downstream_gene_variant MODIFIER c.*1719G>A| S219
101724 BAA10g07300 A10 4149191 C T downstream_gene_variant MODIFIER c.*1957C>T| S19
101725 BAA10g07300 A10 4149533 C T downstream_gene_variant MODIFIER c.*2299C>T| S96