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
179901 BAA02g20070 A02 10577621 C T downstream_gene_variant MODIFIER c.*67C>T| S114
179902 BAA02g20070 A02 10579620 C T downstream_gene_variant MODIFIER c.*2066C>T| S242
179903 BAA02g20070 A02 10579990 C T downstream_gene_variant MODIFIER c.*2436C>T| S177
179904 BAA02g20070 A02 10580600 C T downstream_gene_variant MODIFIER c.*3046C>T| S178
179905 BAA02g20070 A02 10581709 G A downstream_gene_variant MODIFIER c.*4155G>A| S152
179906 BAA02g20080 A02 10582783 G A splice_region_variant&intron_variant LOW c.655-6C>T| S197
179907 BAA02g20080 A02 10582931 C T synonymous_variant LOW c.585G>A|p.Leu195Leu S301
S304
179908 BAA02g20080 A02 10583069 G A synonymous_variant LOW c.447C>T|p.Leu149Leu S282
179909 BAA02g20080 A02 10583073 G A missense_variant MODERATE c.443C>T|p.Ser148Phe S28
179910 BAA02g20080 A02 10583152 G A intron_variant MODIFIER c.388-24C>T| S107
179911 BAA02g20080 A02 10584055 C T intron_variant MODIFIER c.388-927G>A| S40
S49
179912 BAA02g20080 A02 10584382 C T intron_variant MODIFIER c.388-1254G>A| S163
S183
S198
179913 BAA02g20080 A02 10584407 C G intron_variant MODIFIER c.388-1279G>C| S109
179914 BAA02g20080 A02 10584459 C T intron_variant MODIFIER c.388-1331G>A| S51
179915 BAA02g20080 A02 10586416 C T intron_variant MODIFIER c.387+1016G>A| S270
179916 BAA02g20080 A02 10587833 C T intron_variant MODIFIER c.100-114G>A| S82
S92
179917 BAA02g20090 A02 10594888 C T upstream_gene_variant MODIFIER c.-477C>T| S5
179918 BAA02g20090 A02 10595351 C T upstream_gene_variant MODIFIER c.-14C>T| S138
179919 BAA02g20090 A02 10595408 C T missense_variant MODERATE c.44C>T|p.Ser15Phe S114
179920 BAA02g20090 A02 10595499 C T synonymous_variant LOW c.135C>T|p.Ser45Ser S142
179921 BAA02g20090 A02 10595571 C T synonymous_variant LOW c.207C>T|p.Gly69Gly S203
179922 BAA02g20090 A02 10595658 G A synonymous_variant LOW c.294G>A|p.Glu98Glu S143
179923 BAA02g20090 A02 10595730 C T synonymous_variant LOW c.366C>T|p.Thr122Thr S9
179924 BAA02g20090 A02 10596034 C T synonymous_variant LOW c.670C>T|p.Leu224Leu S75
S81
179925 BAA02g20090 A02 10596142 G A missense_variant MODERATE c.778G>A|p.Glu260Lys S134