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
103601 BAA10g07800 A10 4800140 C T upstream_gene_variant MODIFIER c.-4008C>T| S249
103602 BAA10g07800 A10 4800283 C T upstream_gene_variant MODIFIER c.-3865C>T| S135
103603 BAA10g07790 A10 4800817 C T upstream_gene_variant MODIFIER c.-78G>A| S282
103604 BAA10g07790 A10 4801359 C T upstream_gene_variant MODIFIER c.-620G>A| S9
103605 BAA10g07790 A10 4802059 C T upstream_gene_variant MODIFIER c.-1320G>A| S177
103606 BAA10g07790 A10 4802847 C T upstream_gene_variant MODIFIER c.-2108G>A| S40
S49
103607 BAA10g07790 A10 4803148 G A upstream_gene_variant MODIFIER c.-2409C>T| S1
103608 BAA10g07790 A10 4803421 C T upstream_gene_variant MODIFIER c.-2682G>A| S173
103609 BAA10g07790 A10 4804034 C T upstream_gene_variant MODIFIER c.-3295G>A| S295
103610 BAA10g07800 A10 4804512 T C missense_variant MODERATE c.274T>C|p.Phe92Leu S84
S93
103611 BAA10g07800 A10 4805304 C T missense_variant MODERATE c.656C>T|p.Ala219Val S225
S73
103612 BAA10g07800 A10 4805403 C T missense_variant MODERATE c.755C>T|p.Pro252Leu S61
103613 BAA10g07790 A10 4805450 C T upstream_gene_variant MODIFIER c.-4711G>A| S132
S137
S215
103614 BAA10g07800 A10 4806391 G A downstream_gene_variant MODIFIER c.*945G>A| S151
S216
S263
103615 BAA10g07800 A10 4807627 C T downstream_gene_variant MODIFIER c.*2181C>T| S8
103616 BAA10g07800 A10 4807668 C T downstream_gene_variant MODIFIER c.*2222C>T| S246
103617 BAA10g07800 A10 4807925 C T downstream_gene_variant MODIFIER c.*2479C>T| S270
103618 BAA10g07800 A10 4808152 C T downstream_gene_variant MODIFIER c.*2706C>T| S2
103619 BAA10g07800 A10 4808867 G A downstream_gene_variant MODIFIER c.*3421G>A| S138
103620 BAA10g07800 A10 4809424 G A downstream_gene_variant MODIFIER c.*3978G>A| S12
103621 BAA10g07800 A10 4809831 G A downstream_gene_variant MODIFIER c.*4385G>A| S127
103622 BAA10g07800 A10 4809855 G A downstream_gene_variant MODIFIER c.*4409G>A| S289
103623 BAA10g07800 A10 4809871 G A downstream_gene_variant MODIFIER c.*4425G>A| S151
S263
103624 BAA10g07800 A10 4810023 G A downstream_gene_variant MODIFIER c.*4577G>A| S201
103625 BAA10g07800 A10 4810119 G A downstream_gene_variant MODIFIER c.*4673G>A| S59