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
117901 BAA10g10780-BAA10g10790 A10 12530896 C T intergenic_region MODIFIER n.12530896C>T| S187
117902 BAA10g10780-BAA10g10790 A10 12530924 C T intergenic_region MODIFIER n.12530924C>T| S124
117903 BAA10g10790 A10 12532342 A C downstream_gene_variant MODIFIER c.*4917T>G| S284
117904 BAA10g10790 A10 12532688 C T downstream_gene_variant MODIFIER c.*4571G>A| S142
117905 BAA10g10790 A10 12534489 C T downstream_gene_variant MODIFIER c.*2770G>A| S5
117906 BAA10g10790 A10 12535331 G A downstream_gene_variant MODIFIER c.*1928C>T| S161
117907 BAA10g10790 A10 12535336 C T downstream_gene_variant MODIFIER c.*1923G>A| S12
117908 BAA10g10790 A10 12536859 C T downstream_gene_variant MODIFIER c.*400G>A| S68
117909 BAA10g10790 A10 12537123 C G downstream_gene_variant MODIFIER c.*136G>C| S104
S131
S136
S157
S178
S207
S258
S275
S283
S286
S289
117910 BAA10g10790 A10 12537275 C T missense_variant MODERATE c.2081G>A|p.Arg694Lys S206
S26
117911 BAA10g10790 A10 12537492 G A missense_variant MODERATE c.2011C>T|p.Pro671Ser S288
117912 BAA10g10790 A10 12538365 C T intron_variant MODIFIER c.1434-35G>A| S70
117913 BAA10g10790 A10 12539260 C T missense_variant MODERATE c.961G>A|p.Gly321Arg S270
117914 BAA10g10790 A10 12539884 G A intron_variant MODIFIER c.769+23C>T| S11
117915 BAA10g10790 A10 12539981 C T missense_variant MODERATE c.695G>A|p.Gly232Asp S117
117916 BAA10g10790 A10 12541635 G A intron_variant MODIFIER c.562-1521C>T| S295
117917 BAA10g10790 A10 12541744 G A intron_variant MODIFIER c.562-1630C>T| S100
117918 BAA10g10790 A10 12542066 G T intron_variant MODIFIER c.562-1952C>A| S221
117919 BAA10g10790 A10 12542415 G A intron_variant MODIFIER c.562-2301C>T| S136
117920 BAA10g10790 A10 12542571 G A intron_variant MODIFIER c.562-2457C>T| S262
117921 BAA10g10790 A10 12546001 G A intron_variant MODIFIER c.561+3041C>T| S184
117922 BAA10g10790 A10 12546446 C T intron_variant MODIFIER c.561+2596G>A| S199
117923 BAA10g10790 A10 12547744 C T intron_variant MODIFIER c.561+1298G>A| S73
S91
117924 BAA10g10800 A10 12548189 C T upstream_gene_variant MODIFIER c.-4629C>T| S76
117925 BAA10g10800 A10 12548486 C T upstream_gene_variant MODIFIER c.-4332C>T| S276