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
151851 BAA02g00460 A02 254777 G A upstream_gene_variant MODIFIER c.-1868G>A| S125
151852 BAA02g00460 A02 255220 C T upstream_gene_variant MODIFIER c.-1425C>T| S242
151853 BAA02g00460 A02 255666 C T upstream_gene_variant MODIFIER c.-979C>T| S99
151854 BAA02g00460 A02 256629 C T upstream_gene_variant MODIFIER c.-16C>T| S40
S49
151855 BAA02g00460 A02 256761 C T synonymous_variant LOW c.117C>T|p.His39His S133
151856 BAA02g00460 A02 256935 G A missense_variant MODERATE c.202G>A|p.Val68Met S125
151857 BAA02g00460 A02 257954 G A missense_variant MODERATE c.607G>A|p.Gly203Ser S279
151858 BAA02g00460 A02 258143 G A downstream_gene_variant MODIFIER c.*10G>A| S48
151859 BAA02g00470 A02 261215 C T missense_variant MODERATE c.433G>A|p.Glu145Lys S112
151860 BAA02g00470 A02 261618 C T missense_variant MODERATE c.133G>A|p.Gly45Arg S233
151861 BAA02g00480 A02 267168 G A downstream_gene_variant MODIFIER c.*3286C>T| S177
151862 BAA02g00490 A02 268546 C T upstream_gene_variant MODIFIER c.-4880C>T| S159
151863 BAA02g00490 A02 268666 G A upstream_gene_variant MODIFIER c.-4760G>A| S273
151864 BAA02g00490 A02 269979 C T upstream_gene_variant MODIFIER c.-3447C>T| S192
151865 BAA02g00490 A02 270680 C T upstream_gene_variant MODIFIER c.-2746C>T| S251
151866 BAA02g00490 A02 270870 C T upstream_gene_variant MODIFIER c.-2556C>T| S123
151867 BAA02g00480 A02 271801 G A synonymous_variant LOW c.9C>T|p.Val3Val S169
151868 BAA02g00480 A02 271976 G A upstream_gene_variant MODIFIER c.-167C>T| S286
151869 BAA02g00480 A02 272242 G A upstream_gene_variant MODIFIER c.-433C>T| S28
151870 BAA02g00480 A02 272785 T C upstream_gene_variant MODIFIER c.-976A>G| S107
151871 BAA02g00490 A02 273650 G A synonymous_variant LOW c.153G>A|p.Glu51Glu S292
151872 BAA02g00490 A02 273774 G A missense_variant MODERATE c.277G>A|p.Glu93Lys S5
151873 BAA02g00490 A02 273829 G A missense_variant MODERATE c.332G>A|p.Gly111Asp S291
151874 BAA02g00490 A02 274178 C T synonymous_variant LOW c.681C>T|p.Leu227Leu S172
S217
151875 BAA02g00490 A02 274878 G A synonymous_variant LOW c.1245G>A|p.Glu415Glu S170