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
173801 BAA02g16930 A02 8391869 G A downstream_gene_variant MODIFIER c.*418C>T| S295
173802 BAA02g16930 A02 8392010 G T downstream_gene_variant MODIFIER c.*277C>A| S164
173803 BAA02g16930 A02 8392125 G A downstream_gene_variant MODIFIER c.*162C>T| S132
S215
173804 BAA02g16930 A02 8392314 C T synonymous_variant LOW c.276G>A|p.Ser92Ser S13
173805 BAA02g16930 A02 8392627 C T upstream_gene_variant MODIFIER c.-38G>A| S84
S93
173806 BAA02g16930 A02 8393894 G A upstream_gene_variant MODIFIER c.-1305C>T| S20
173807 BAA02g16940 A02 8395501 G A missense_variant MODERATE c.2746C>T|p.Pro916Ser S94
173808 BAA02g16940 A02 8396376 C T missense_variant MODERATE c.2026G>A|p.Asp676Asn S267
173809 BAA02g16930 A02 8396529 C T upstream_gene_variant MODIFIER c.-3940G>A| S255
173810 BAA02g16940 A02 8396635 C T missense_variant MODERATE c.1921G>A|p.Asp641Asn S302
173811 BAA02g16940 A02 8397135 G A synonymous_variant LOW c.1512C>T|p.Phe504Phe S105
S106
173812 BAA02g16940 A02 8397245 C T missense_variant MODERATE c.1402G>A|p.Glu468Lys S116
173813 BAA02g16940 A02 8398019 G A synonymous_variant LOW c.798C>T|p.Ser266Ser S37
173814 BAA02g16940 A02 8398102 G A missense_variant MODERATE c.715C>T|p.Leu239Phe S2
173815 BAA02g16940 A02 8398511 C T intron_variant MODIFIER c.579-273G>A| S238
173816 BAA02g16940 A02 8398514 G A intron_variant MODIFIER c.579-276C>T| S257
173817 BAA02g16940 A02 8399616 C T upstream_gene_variant MODIFIER c.-41G>A| S220
S5
173818 BAA02g16940 A02 8399952 C T upstream_gene_variant MODIFIER c.-377G>A| S138
173819 BAA02g16940 A02 8401028 C T upstream_gene_variant MODIFIER c.-1453G>A| S224
173820 BAA02g16940 A02 8401071 G A upstream_gene_variant MODIFIER c.-1496C>T| S247
173821 BAA02g16940 A02 8402255 G A upstream_gene_variant MODIFIER c.-2680C>T| S74
173822 BAA02g16940 A02 8404218 G A upstream_gene_variant MODIFIER c.-4643C>T| S4
173823 BAA02g16960 A02 8404867 C T missense_variant MODERATE c.1538G>A|p.Gly513Glu S55
173824 BAA02g16950 A02 8404983 G A downstream_gene_variant MODIFIER c.*863G>A| S287
173825 BAA02g16960 A02 8405272 C T missense_variant MODERATE c.1315G>A|p.Ala439Thr S123