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
173751 BAA02g16920 A02 8376140 G A upstream_gene_variant MODIFIER c.-3918G>A| S95
173752 BAA02g16920 A02 8376319 G A upstream_gene_variant MODIFIER c.-3739G>A| S272
173753 BAA02g16920 A02 8377186 C T upstream_gene_variant MODIFIER c.-2872C>T| S9
173754 BAA02g16920 A02 8377627 G A upstream_gene_variant MODIFIER c.-2431G>A| S274
173755 BAA02g16920 A02 8377978 C T upstream_gene_variant MODIFIER c.-2080C>T| S78
173756 BAA02g16920 A02 8378145 C T upstream_gene_variant MODIFIER c.-1913C>T| S92
173757 BAA02g16920 A02 8379499 C T upstream_gene_variant MODIFIER c.-559C>T| S81
S85
173758 BAA02g16920 A02 8379776 G A upstream_gene_variant MODIFIER c.-282G>A| S269
173759 BAA02g16920 A02 8380113 C T missense_variant MODERATE c.56C>T|p.Ser19Leu S275
173760 BAA02g16920 A02 8380483 C T synonymous_variant LOW c.426C>T|p.Thr142Thr S208
S219
173761 BAA02g16920 A02 8380828 G A synonymous_variant LOW c.771G>A|p.Glu257Glu S197
173762 BAA02g16920 A02 8381483 G A downstream_gene_variant MODIFIER c.*412G>A| S43
173763 BAA02g16920 A02 8381993 C T downstream_gene_variant MODIFIER c.*922C>T| S65
173764 BAA02g16920 A02 8382229 C T downstream_gene_variant MODIFIER c.*1158C>T| S13
173765 BAA02g16920 A02 8382524 G A downstream_gene_variant MODIFIER c.*1453G>A| S157
173766 BAA02g16920 A02 8383379 C T downstream_gene_variant MODIFIER c.*2308C>T| S241
173767 BAA02g16920 A02 8383435 C T downstream_gene_variant MODIFIER c.*2364C>T| S268
173768 BAA02g16920 A02 8384849 G A downstream_gene_variant MODIFIER c.*3778G>A| S170
173769 BAA02g16920 A02 8385943 G A downstream_gene_variant MODIFIER c.*4872G>A| S149
173770 BAA02g16920-BAA02g16930 A02 8387272 G A intergenic_region MODIFIER n.8387272G>A| S4
173771 BAA02g16930 A02 8388501 G A downstream_gene_variant MODIFIER c.*3786C>T| S62
173772 BAA02g16930 A02 8391105 C T downstream_gene_variant MODIFIER c.*1182G>A| S18
173773 BAA02g16930 A02 8391716 C T downstream_gene_variant MODIFIER c.*571G>A| S179
173774 BAA02g16930 A02 8391768 G A downstream_gene_variant MODIFIER c.*519C>T| S146
173775 BAA02g16930 A02 8391786 C T downstream_gene_variant MODIFIER c.*501G>A| S245