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
132701 BAA10g19510-BAA10g19520 A10 17866514 G A intergenic_region MODIFIER n.17866514G>A| S162
132702 BAA10g19510-BAA10g19520 A10 17866795 C T intergenic_region MODIFIER n.17866795C>T| S272
132703 BAA10g19520 A10 17867395 C T downstream_gene_variant MODIFIER c.*4909G>A| S68
132704 BAA10g19520 A10 17870024 G A downstream_gene_variant MODIFIER c.*2280C>T| S261
132705 BAA10g19520 A10 17870237 C T downstream_gene_variant MODIFIER c.*2067G>A| S25
132706 BAA10g19520 A10 17870651 G A downstream_gene_variant MODIFIER c.*1653C>T| S158
132707 BAA10g19520 A10 17870808 G A downstream_gene_variant MODIFIER c.*1496C>T| S250
132708 BAA10g19520 A10 17871202 G A downstream_gene_variant MODIFIER c.*1102C>T| S270
132709 BAA10g19520 A10 17871538 G A downstream_gene_variant MODIFIER c.*766C>T| S240
132710 BAA10g19520 A10 17872175 C T downstream_gene_variant MODIFIER c.*129G>A| S186
132711 BAA10g19520 A10 17872224 C T downstream_gene_variant MODIFIER c.*80G>A| S83
S88
132712 BAA10g19520 A10 17872248 G A downstream_gene_variant MODIFIER c.*56C>T| S174
S27
132713 BAA10g19520 A10 17872666 C T missense_variant MODERATE c.289G>A|p.Asp97Asn S157
132714 BAA10g19520 A10 17872711 C T intron_variant MODIFIER c.274-30G>A| S114
132715 BAA10g19520 A10 17872723 C T intron_variant MODIFIER c.274-42G>A| S282
132716 BAA10g19520 A10 17874059 G A intron_variant MODIFIER c.274-1378C>T| S132
S137
S215
S288
S89
132717 BAA10g19530 A10 17875353 C T downstream_gene_variant MODIFIER c.*4441G>A| S209
132718 BAA10g19530 A10 17875362 G A downstream_gene_variant MODIFIER c.*4432C>T| S142
132719 BAA10g19530 A10 17875410 G A downstream_gene_variant MODIFIER c.*4384C>T| S142
132720 BAA10g19530 A10 17875789 G A downstream_gene_variant MODIFIER c.*4005C>T| S162
132721 BAA10g19530 A10 17875805 G A downstream_gene_variant MODIFIER c.*3989C>T| S61
132722 BAA10g19530 A10 17875926 C T downstream_gene_variant MODIFIER c.*3868G>A| S38
132723 BAA10g19530 A10 17875987 C T downstream_gene_variant MODIFIER c.*3807G>A| S166
132724 BAA10g19530 A10 17876272 G A downstream_gene_variant MODIFIER c.*3522C>T| S197
132725 BAA10g19530 A10 17876375 C T downstream_gene_variant MODIFIER c.*3419G>A| S199