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
171901 BAA02g15870 A02 7725101 G T synonymous_variant LOW c.1740G>T|p.Val580Val S245
171902 BAA02g15870 A02 7725240 G A missense_variant MODERATE c.1879G>A|p.Ala627Thr S158
171903 BAA02g15870 A02 7725247 G A missense_variant MODERATE c.1886G>A|p.Arg629Lys S282
171904 BAA02g15870 A02 7726442 G A downstream_gene_variant MODIFIER c.*945G>A| S52
171905 BAA02g15880 A02 7726737 C T missense_variant MODERATE c.440G>A|p.Gly147Asp S272
171906 BAA02g15870 A02 7727547 A G downstream_gene_variant MODIFIER c.*2050A>G| S301
S304
171907 BAA02g15880 A02 7727982 C T upstream_gene_variant MODIFIER c.-240G>A| S171
171908 BAA02g15880 A02 7729599 C T upstream_gene_variant MODIFIER c.-1857G>A| S114
171909 BAA02g15880 A02 7729622 G A upstream_gene_variant MODIFIER c.-1880C>T| S280
171910 BAA02g15890 A02 7734703 G A intron_variant MODIFIER c.703+800C>T| S4
171911 BAA02g15890 A02 7734835 G A intron_variant MODIFIER c.703+668C>T| S291
171912 BAA02g15890 A02 7735642 C T synonymous_variant LOW c.564G>A|p.Val188Val S46
171913 BAA02g15890 A02 7735717 G A synonymous_variant LOW c.489C>T|p.Tyr163Tyr S159
S243
171914 BAA02g15890 A02 7735973 C T missense_variant MODERATE c.233G>A|p.Gly78Asp S128
171915 BAA02g15890 A02 7736227 G A upstream_gene_variant MODIFIER c.-22C>T| S17
171916 BAA02g15890 A02 7736743 C T upstream_gene_variant MODIFIER c.-538G>A| S255
171917 BAA02g15890 A02 7737801 C T upstream_gene_variant MODIFIER c.-1596G>A| S178
171918 BAA02g15890 A02 7738168 G A upstream_gene_variant MODIFIER c.-1963C>T| S264
171919 BAA02g15890 A02 7739260 G A upstream_gene_variant MODIFIER c.-3055C>T| S298
171920 BAA02g15890 A02 7740848 G A upstream_gene_variant MODIFIER c.-4643C>T| S305
171921 BAA02g15890 A02 7740958 C T upstream_gene_variant MODIFIER c.-4753G>A| S144
171922 BAA02g15900 A02 7741231 C T downstream_gene_variant MODIFIER c.*2078G>A| S142
171923 BAA02g15900 A02 7741262 C A downstream_gene_variant MODIFIER c.*2047G>T| S57
171924 BAA02g15900 A02 7743422 C T missense_variant MODERATE c.1012G>A|p.Ala338Thr S55
171925 BAA02g15900 A02 7745178 C A missense_variant MODERATE c.202G>T|p.Gly68Cys S44