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
218851 BAA02g33030 A02 28294981 C T downstream_gene_variant MODIFIER c.*3413G>A| S94
218852 BAA02g33030 A02 28297335 C T downstream_gene_variant MODIFIER c.*1059G>A| S261
218853 BAA02g33030 A02 28297390 G A downstream_gene_variant MODIFIER c.*1004C>T| S174
218854 BAA02g33030 A02 28297796 C T downstream_gene_variant MODIFIER c.*598G>A| S65
218855 BAA02g33030 A02 28298483 C T missense_variant MODERATE c.709G>A|p.Gly237Ser S277
218856 BAA02g33030 A02 28299007 G A missense_variant MODERATE c.358C>T|p.Pro120Ser S47
218857 BAA02g33030 A02 28299274 C T missense_variant MODERATE c.208G>A|p.Val70Ile S273
218858 BAA02g33030 A02 28300806 G A upstream_gene_variant MODIFIER c.-1216C>T| S150
218859 BAA02g33030 A02 28301310 C T upstream_gene_variant MODIFIER c.-1720G>A| S284
218860 BAA02g33030 A02 28301486 G A upstream_gene_variant MODIFIER c.-1896C>T| S269
218861 BAA02g33030 A02 28301678 G A upstream_gene_variant MODIFIER c.-2088C>T| S297
218862 BAA02g33030 A02 28301819 G A upstream_gene_variant MODIFIER c.-2229C>T| S238
218863 BAA02g33030 A02 28301884 G A upstream_gene_variant MODIFIER c.-2294C>T| S98
218864 BAA02g33030 A02 28302081 T C upstream_gene_variant MODIFIER c.-2491A>G| S282
218865 BAA02g33030 A02 28302546 G A upstream_gene_variant MODIFIER c.-2956C>T| S268
218866 BAA02g33030 A02 28302693 G A upstream_gene_variant MODIFIER c.-3103C>T| S256
218867 BAA02g33040 A02 28304680 G A downstream_gene_variant MODIFIER c.*403G>A| S148
S210
S30
S31
218868 BAA02g33040 A02 28305366 G A downstream_gene_variant MODIFIER c.*1089G>A| S143
218869 BAA02g33040 A02 28306344 G A downstream_gene_variant MODIFIER c.*2067G>A| S278
218870 BAA02g33040 A02 28306485 C T downstream_gene_variant MODIFIER c.*2208C>T| S15
S3
218871 BAA02g33040 A02 28306610 T A downstream_gene_variant MODIFIER c.*2333T>A| S266
218872 BAA02g33040 A02 28306845 C T downstream_gene_variant MODIFIER c.*2568C>T| S25
S264
218873 BAA02g33050 A02 28309440 C T intron_variant MODIFIER c.1076+117G>A| S115
218874 BAA02g33050 A02 28310051 C T missense_variant MODERATE c.754G>A|p.Gly252Arg S296
218875 BAA02g33050 A02 28310283 G A intron_variant MODIFIER c.631-32C>T| S95