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
94901 BAA10g03760 A10 1819868 G A upstream_gene_variant MODIFIER c.-1471C>T| S286
94902 BAA10g03760 A10 1820269 C T upstream_gene_variant MODIFIER c.-1872G>A| S139
94903 BAA10g03760 A10 1822204 G A upstream_gene_variant MODIFIER c.-3807C>T| S290
94904 BAA10g03760 A10 1822473 G A upstream_gene_variant MODIFIER c.-4076C>T| S126
94905 BAA10g03770 A10 1825776 C T upstream_gene_variant MODIFIER c.-3295C>T| S47
94906 BAA10g03770 A10 1826376 C T upstream_gene_variant MODIFIER c.-2695C>T| S225
S73
94907 BAA10g03770 A10 1826597 C T upstream_gene_variant MODIFIER c.-2474C>T| S47
94908 BAA10g03770 A10 1827288 C T upstream_gene_variant MODIFIER c.-1783C>T| S226
94909 BAA10g03770 A10 1827550 C T upstream_gene_variant MODIFIER c.-1521C>T| S121
94910 BAA10g03770 A10 1827602 C T upstream_gene_variant MODIFIER c.-1469C>T| S226
94911 BAA10g03770 A10 1827797 C T upstream_gene_variant MODIFIER c.-1274C>T| S298
94912 BAA10g03770 A10 1827919 G A upstream_gene_variant MODIFIER c.-1152G>A| S36
94913 BAA10g03770 A10 1828735 G A upstream_gene_variant MODIFIER c.-336G>A| S245
94914 BAA10g03770 A10 1829291 C T missense_variant MODERATE c.221C>T|p.Pro74Leu S61
94915 BAA10g03770 A10 1829412 G A splice_region_variant&intron_variant LOW c.267-7G>A| S303
94916 BAA10g03770 A10 1829488 C T synonymous_variant LOW c.336C>T|p.Phe112Phe S224
94917 BAA10g03780 A10 1830477 C T downstream_gene_variant MODIFIER c.*1885G>A| S123
94918 BAA10g03780 A10 1830585 G A downstream_gene_variant MODIFIER c.*1777C>T| S36
94919 BAA10g03780 A10 1832436 C T missense_variant MODERATE c.892G>A|p.Glu298Lys S208
S93
94920 BAA10g03780 A10 1835010 C T upstream_gene_variant MODIFIER c.-1345G>A| S88
94921 BAA10g03780 A10 1835044 G A upstream_gene_variant MODIFIER c.-1379C>T| S55
94922 BAA10g03780 A10 1835188 C T upstream_gene_variant MODIFIER c.-1523G>A| S249
94923 BAA10g03780 A10 1836912 G A upstream_gene_variant MODIFIER c.-3247C>T| S161
94924 BAA10g03790 A10 1839101 A G missense_variant MODERATE c.1643T>C|p.Met548Thr S77
S82
94925 BAA10g03790 A10 1839851 G A missense_variant MODERATE c.893C>T|p.Thr298Met S55