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
152901 BAA02g01390 A02 648177 G A upstream_gene_variant MODIFIER c.-4123C>T| S206
S26
152902 BAA02g01420 A02 649130 G A upstream_gene_variant MODIFIER c.-1173G>A| S146
152903 BAA02g01420 A02 649655 G A upstream_gene_variant MODIFIER c.-648G>A| S59
152904 BAA02g01420 A02 649797 C T upstream_gene_variant MODIFIER c.-506C>T| S228
152905 BAA02g01420 A02 651298 G A synonymous_variant LOW c.996G>A|p.Lys332Lys S169
152906 BAA02g01430 A02 651720 C T upstream_gene_variant MODIFIER c.-1818C>T| S71
152907 BAA02g01430 A02 652688 C T upstream_gene_variant MODIFIER c.-850C>T| S262
152908 BAA02g01430 A02 653005 G A upstream_gene_variant MODIFIER c.-533G>A| S295
152909 BAA02g01430 A02 653603 C T synonymous_variant LOW c.66C>T|p.Leu22Leu S200
152910 BAA02g01430 A02 653995 C T missense_variant MODERATE c.394C>T|p.His132Tyr S121
152911 BAA02g01430 A02 655197 G A missense_variant MODERATE c.1198G>A|p.Ala400Thr S263
152912 BAA02g01420 A02 655614 G A downstream_gene_variant MODIFIER c.*4253G>A| S139
152913 BAA02g01440 A02 656246 C T missense_variant MODERATE c.685G>A|p.Val229Met S15
152914 BAA02g01430 A02 656564 G A downstream_gene_variant MODIFIER c.*1050G>A| S171
152915 BAA02g01430 A02 656712 C T downstream_gene_variant MODIFIER c.*1198C>T| S251
152916 BAA02g01430 A02 657284 G A downstream_gene_variant MODIFIER c.*1770G>A| S221
152917 BAA02g01430 A02 657710 C T downstream_gene_variant MODIFIER c.*2196C>T| S201
152918 BAA02g01440 A02 658371 G A upstream_gene_variant MODIFIER c.-208C>T| S236
152919 BAA02g01440 A02 658561 C T upstream_gene_variant MODIFIER c.-398G>A| S87
152920 BAA02g01440 A02 658611 G A upstream_gene_variant MODIFIER c.-448C>T| S265
152921 BAA02g01440 A02 659555 G A upstream_gene_variant MODIFIER c.-1392C>T| S206
S26
152922 BAA02g01440 A02 662302 G A upstream_gene_variant MODIFIER c.-4139C>T| S179
152923 BAA02g01460 A02 663633 C T downstream_gene_variant MODIFIER c.*1467G>A| S201
152924 BAA02g01460 A02 663914 G A downstream_gene_variant MODIFIER c.*1186C>T| S166
152925 BAA02g01460 A02 664403 G A downstream_gene_variant MODIFIER c.*697C>T| S33