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
152851 BAA02g01380 A02 629725 G A upstream_gene_variant MODIFIER c.-894C>T| S132
S137
S162
S89
152852 BAA02g01380 A02 633278 G A upstream_gene_variant MODIFIER c.-4447C>T| S35
152853 BAA02g01380-BAA02g01390 A02 634183 G A intergenic_region MODIFIER n.634183G>A| S139
152854 BAA02g01380-BAA02g01390 A02 634227 G A intergenic_region MODIFIER n.634227G>A| S25
152855 BAA02g01380-BAA02g01390 A02 634294 G A intergenic_region MODIFIER n.634294G>A| S184
152856 BAA02g01380-BAA02g01390 A02 634365 G A intergenic_region MODIFIER n.634365G>A| S25
152857 BAA02g01380-BAA02g01390 A02 634431 C T intergenic_region MODIFIER n.634431C>T| S270
152858 BAA02g01390 A02 640923 G A downstream_gene_variant MODIFIER c.*1698C>T| S17
152859 BAA02g01390 A02 641038 G A downstream_gene_variant MODIFIER c.*1583C>T| S217
S248
152860 BAA02g01400 A02 641409 G A upstream_gene_variant MODIFIER c.-4799G>A| S86
152861 BAA02g01400 A02 641817 C T upstream_gene_variant MODIFIER c.-4391C>T| S13
152862 BAA02g01390 A02 642631 C T missense_variant MODERATE c.572G>A|p.Ser191Asn S262
152863 BAA02g01390 A02 642726 G A synonymous_variant LOW c.477C>T|p.Leu159Leu S168
152864 BAA02g01400 A02 642849 G A upstream_gene_variant MODIFIER c.-3359G>A| S169
152865 BAA02g01390 A02 643670 C T missense_variant MODERATE c.133G>A|p.Gly45Arg S28
152866 BAA02g01400 A02 643825 C T upstream_gene_variant MODIFIER c.-2383C>T| S108
152867 BAA02g01390 A02 644163 C T upstream_gene_variant MODIFIER c.-109G>A| S270
152868 BAA02g01390 A02 644170 G A upstream_gene_variant MODIFIER c.-116C>T| S169
152869 BAA02g01390 A02 644194 G A upstream_gene_variant MODIFIER c.-140C>T| S132
S137
S215
S89
152870 BAA02g01390 A02 644653 C T upstream_gene_variant MODIFIER c.-599G>A| S242
152871 BAA02g01390 A02 645315 G A upstream_gene_variant MODIFIER c.-1261C>T| S287
S293
152872 BAA02g01410 A02 647420 C T synonymous_variant LOW c.147C>T|p.Cys49Cys S187
152873 BAA02g01410 A02 647787 G A missense_variant MODERATE c.430G>A|p.Gly144Ser S202
152874 BAA02g01390 A02 647970 C T upstream_gene_variant MODIFIER c.-3916G>A| S270
152875 BAA02g01390 A02 648034 G A upstream_gene_variant MODIFIER c.-3980C>T| S276