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
185601 BAA02g23140 A02 12618268 C T missense_variant MODERATE c.1103C>T|p.Thr368Ile S221
185602 BAA02g23140 A02 12618861 G A missense_variant MODERATE c.1262G>A|p.Gly421Glu S72
S78
185603 BAA02g23140 A02 12619123 G A synonymous_variant LOW c.1524G>A|p.Lys508Lys S282
185604 BAA02g23150 A02 12619989 C T missense_variant MODERATE c.493G>A|p.Glu165Lys S293
185605 BAA02g23150 A02 12621315 C T upstream_gene_variant MODIFIER c.-834G>A| S192
185606 BAA02g23150 A02 12621622 G A upstream_gene_variant MODIFIER c.-1141C>T| S196
185607 BAA02g23150 A02 12622012 C T upstream_gene_variant MODIFIER c.-1531G>A| S171
185608 BAA02g23150 A02 12622201 G A upstream_gene_variant MODIFIER c.-1720C>T| S134
185609 BAA02g23150 A02 12622356 G A upstream_gene_variant MODIFIER c.-1875C>T| S134
185610 BAA02g23160 A02 12625570 G A downstream_gene_variant MODIFIER c.*1558G>A| S229
185611 BAA02g23160 A02 12627761 G A downstream_gene_variant MODIFIER c.*3749G>A| S48
185612 BAA02g23170 A02 12629277 C T downstream_gene_variant MODIFIER c.*565G>A| S8
185613 BAA02g23170 A02 12629993 G A missense_variant MODERATE c.728C>T|p.Thr243Ile S99
185614 BAA02g23170 A02 12630813 G A splice_region_variant&synonymous_variant LOW c.162C>T|p.Asp54Asp S17
185615 BAA02g23170 A02 12634500 C T upstream_gene_variant MODIFIER c.-3386G>A| S42
185616 BAA02g23170 A02 12635029 C T upstream_gene_variant MODIFIER c.-3915G>A| S292
185617 BAA02g23170 A02 12635734 G A upstream_gene_variant MODIFIER c.-4620C>T| S113
185618 BAA02g23170 A02 12636109 C T upstream_gene_variant MODIFIER c.-4995G>A| S33
185619 BAA02g23170-BAA02g23180 A02 12636636 G A intergenic_region MODIFIER n.12636636G>A| S261
S303
185620 BAA02g23180 A02 12640385 C T upstream_gene_variant MODIFIER c.-1829C>T| S273
185621 BAA02g23180 A02 12641772 C T upstream_gene_variant MODIFIER c.-442C>T| S249
185622 BAA02g23180 A02 12641876 C T upstream_gene_variant MODIFIER c.-338C>T| S80
185623 BAA02g23210 A02 12643274 C T upstream_gene_variant MODIFIER c.-4620C>T| S205
185624 BAA02g23190 A02 12644159 C T splice_acceptor_variant&intron_variant HIGH c.223-1G>A| S302
185625 BAA02g23200 A02 12645619 C T missense_variant MODERATE c.1348G>A|p.Asp450Asn S179