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
217851 BAA02g32740 A02 27973390 G A missense_variant MODERATE c.265G>A|p.Glu89Lys S103
217852 BAA02g32740 A02 27974561 G A downstream_gene_variant MODIFIER c.*1127G>A| S166
217853 BAA02g32740 A02 27974774 C T downstream_gene_variant MODIFIER c.*1340C>T| S255
217854 BAA02g32740 A02 27974904 C T downstream_gene_variant MODIFIER c.*1470C>T| S201
217855 BAA02g32740 A02 27974937 G A downstream_gene_variant MODIFIER c.*1503G>A| S69
217856 BAA02g32740 A02 27975693 G A downstream_gene_variant MODIFIER c.*2259G>A| S17
217857 BAA02g32740 A02 27975705 G A downstream_gene_variant MODIFIER c.*2271G>A| S7
217858 BAA02g32740 A02 27976200 C T downstream_gene_variant MODIFIER c.*2766C>T| S172
S217
217859 BAA02g32740 A02 27977113 G A downstream_gene_variant MODIFIER c.*3679G>A| S281
217860 BAA02g32740 A02 27977923 G A downstream_gene_variant MODIFIER c.*4489G>A| S143
217861 BAA02g32750 A02 27979948 G A upstream_gene_variant MODIFIER c.-4793G>A| S122
217862 BAA02g32750 A02 27980589 C T upstream_gene_variant MODIFIER c.-4152C>T| S280
217863 BAA02g32750 A02 27980769 G A upstream_gene_variant MODIFIER c.-3972G>A| S188
217864 BAA02g32750 A02 27981090 C T upstream_gene_variant MODIFIER c.-3651C>T| S219
S72
217865 BAA02g32750 A02 27981849 C T upstream_gene_variant MODIFIER c.-2892C>T| S181
217866 BAA02g32750 A02 27982085 G A upstream_gene_variant MODIFIER c.-2656G>A| S232
217867 BAA02g32750 A02 27982225 G A upstream_gene_variant MODIFIER c.-2516G>A| S71
217868 BAA02g32750 A02 27983495 G A upstream_gene_variant MODIFIER c.-1246G>A| S257
217869 BAA02g32750 A02 27983680 G A upstream_gene_variant MODIFIER c.-1061G>A| S34
217870 BAA02g32750 A02 27984604 G A upstream_gene_variant MODIFIER c.-137G>A| S297
217871 BAA02g32750 A02 27985085 C T synonymous_variant LOW c.345C>T|p.Ala115Ala S19
217872 BAA02g32750 A02 27985981 C T missense_variant MODERATE c.1241C>T|p.Pro414Leu S289
S290
217873 BAA02g32750 A02 27986259 C T intron_variant MODIFIER c.1482+37C>T| S189
217874 BAA02g32750 A02 27986331 G A missense_variant MODERATE c.1489G>A|p.Glu497Lys S168
217875 BAA02g32750 A02 27986352 G A missense_variant MODERATE c.1510G>A|p.Gly504Ser S26