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
122801 BAA10g13010 A10 14268566 C T upstream_gene_variant MODIFIER c.-1237C>T| S297
122802 BAA10g13010 A10 14268601 G A upstream_gene_variant MODIFIER c.-1202G>A| S205
122803 BAA10g13010 A10 14268630 G A upstream_gene_variant MODIFIER c.-1173G>A| S15
122804 BAA10g13010 A10 14269406 G A upstream_gene_variant MODIFIER c.-397G>A| S62
122805 BAA10g13010 A10 14269444 G A upstream_gene_variant MODIFIER c.-359G>A| S100
122806 BAA10g13010 A10 14269896 G A missense_variant MODERATE c.94G>A|p.Asp32Asn S13
122807 BAA10g13000 A10 14270218 G A downstream_gene_variant MODIFIER c.*4084G>A| S151
S263
122808 BAA10g13000 A10 14271052 C T downstream_gene_variant MODIFIER c.*4918C>T| S170
122809 BAA10g13020 A10 14272698 C T downstream_gene_variant MODIFIER c.*4166G>A| S246
122810 BAA10g13020 A10 14275634 C T downstream_gene_variant MODIFIER c.*1230G>A| S259
122811 BAA10g13020 A10 14275925 T C downstream_gene_variant MODIFIER c.*939A>G| S33
122812 BAA10g13020 A10 14277061 C T missense_variant MODERATE c.964G>A|p.Asp322Asn S86
122813 BAA10g13020 A10 14277177 G A missense_variant MODERATE c.848C>T|p.Pro283Leu S128
122814 BAA10g13010 A10 14278314 C T downstream_gene_variant MODIFIER c.*1981C>T| S6
122815 BAA10g13020 A10 14279459 T C missense_variant MODERATE c.556A>G|p.Arg186Gly S266
122816 BAA10g13010 A10 14279553 C T downstream_gene_variant MODIFIER c.*3220C>T| S33
122817 BAA10g13020 A10 14280654 C T synonymous_variant LOW c.48G>A|p.Glu16Glu S42
122818 BAA10g13020 A10 14280831 G A upstream_gene_variant MODIFIER c.-130C>T| S159
122819 BAA10g13020 A10 14285200 G A upstream_gene_variant MODIFIER c.-4499C>T| S118
122820 BAA10g13030 A10 14286456 C T downstream_gene_variant MODIFIER c.*3872G>A| S206
S26
122821 BAA10g13030 A10 14287372 C T downstream_gene_variant MODIFIER c.*2956G>A| S11
122822 BAA10g13030 A10 14288062 C T downstream_gene_variant MODIFIER c.*2266G>A| S12
122823 BAA10g13030 A10 14288077 C T downstream_gene_variant MODIFIER c.*2251G>A| S298
122824 BAA10g13030 A10 14288485 G A downstream_gene_variant MODIFIER c.*1843C>T| S293
122825 BAA10g13030 A10 14289644 C T downstream_gene_variant MODIFIER c.*684G>A| S260