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
115851 BAA10g10010 A10 11809860 C A upstream_gene_variant MODIFIER c.-1813C>A| S284
115852 BAA10g10010 A10 11811513 C T upstream_gene_variant MODIFIER c.-160C>T| S189
115853 BAA10g10010 A10 11811882 C T synonymous_variant LOW c.210C>T|p.Thr70Thr S259
115854 BAA10g10010 A10 11811944 C T missense_variant MODERATE c.272C>T|p.Thr91Ile S17
115855 BAA10g10010 A10 11812883 C T downstream_gene_variant MODIFIER c.*878C>T| S10
115856 BAA10g10020 A10 11813914 C T missense_variant MODERATE c.1180G>A|p.Asp394Asn S83
S88
115857 BAA10g10020 A10 11813964 G A missense_variant MODERATE c.1130C>T|p.Ser377Phe S219
115858 BAA10g10010 A10 11814554 G A downstream_gene_variant MODIFIER c.*2549G>A| S295
115859 BAA10g10020 A10 11814956 G A missense_variant MODERATE c.566C>T|p.Ser189Phe S1
S90
115860 BAA10g10020 A10 11815926 C T missense_variant MODERATE c.103G>A|p.Asp35Asn S11
115861 BAA10g10020 A10 11817267 G A upstream_gene_variant MODIFIER c.-1239C>T| S303
115862 BAA10g10020 A10 11818431 T C upstream_gene_variant MODIFIER c.-2403A>G| S198
115863 BAA10g10020 A10 11818693 C T upstream_gene_variant MODIFIER c.-2665G>A| S51
115864 BAA10g10020 A10 11818826 C T upstream_gene_variant MODIFIER c.-2798G>A| S61
115865 BAA10g10020 A10 11819107 G A upstream_gene_variant MODIFIER c.-3079C>T| S176
115866 BAA10g10020 A10 11820235 G A upstream_gene_variant MODIFIER c.-4207C>T| S159
S243
115867 BAA10g10020 A10 11820396 G A upstream_gene_variant MODIFIER c.-4368C>T| S67
115868 BAA10g10030 A10 11820685 G A synonymous_variant LOW c.1986C>T|p.Pro662Pro S1
S90
115869 BAA10g10030 A10 11820929 C T missense_variant MODERATE c.1742G>A|p.Arg581His S127
115870 BAA10g10030 A10 11821019 G A splice_region_variant&intron_variant LOW c.1658-6C>T| S158
115871 BAA10g10030 A10 11821313 C T synonymous_variant LOW c.1446G>A|p.Lys482Lys S96
115872 BAA10g10030 A10 11821652 G A intron_variant MODIFIER c.1289-14C>T| S161
115873 BAA10g10030 A10 11823674 G A upstream_gene_variant MODIFIER c.-70C>T| S182
115874 BAA10g10030 A10 11823885 C T upstream_gene_variant MODIFIER c.-281G>A| S149
115875 BAA10g10030 A10 11823931 C T upstream_gene_variant MODIFIER c.-327G>A| S237