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
173851 BAA02g16960 A02 8406533 C T missense_variant MODERATE c.301G>A|p.Asp101Asn S131
173852 BAA02g16960 A02 8406562 C T missense_variant MODERATE c.272G>A|p.Gly91Glu S71
173853 BAA02g16950 A02 8406640 G A downstream_gene_variant MODIFIER c.*2520G>A| S187
173854 BAA02g16950 A02 8406902 C T downstream_gene_variant MODIFIER c.*2782C>T| S242
173855 BAA02g16960 A02 8407401 C T upstream_gene_variant MODIFIER c.-54G>A| S108
173856 BAA02g16960 A02 8408420 G A upstream_gene_variant MODIFIER c.-1073C>T| S11
173857 BAA02g16960 A02 8410214 C T upstream_gene_variant MODIFIER c.-2867G>A| S178
173858 BAA02g16960 A02 8410418 G A upstream_gene_variant MODIFIER c.-3071C>T| S19
173859 BAA02g16970 A02 8412718 C T missense_variant MODERATE c.613G>A|p.Gly205Ser S302
173860 BAA02g16970 A02 8414422 G A upstream_gene_variant MODIFIER c.-898C>T| S296
173861 BAA02g16970 A02 8415445 C T upstream_gene_variant MODIFIER c.-1921G>A| S224
173862 BAA02g16970 A02 8415973 C T upstream_gene_variant MODIFIER c.-2449G>A| S159
S188
S243
S276
S298
S299
173863 BAA02g16970 A02 8416305 G A upstream_gene_variant MODIFIER c.-2781C>T| S286
173864 BAA02g16970 A02 8416484 C T upstream_gene_variant MODIFIER c.-2960G>A| S179
173865 BAA02g16970 A02 8416552 C T upstream_gene_variant MODIFIER c.-3028G>A| S66
173866 BAA02g16970 A02 8417759 C T upstream_gene_variant MODIFIER c.-4235G>A| S180
173867 BAA02g16980 A02 8418950 C T downstream_gene_variant MODIFIER c.*1830G>A| S6
173868 BAA02g16980 A02 8419056 C T downstream_gene_variant MODIFIER c.*1724G>A| S233
173869 BAA02g16980 A02 8419652 G A downstream_gene_variant MODIFIER c.*1128C>T| S238
173870 BAA02g16980 A02 8419671 G A downstream_gene_variant MODIFIER c.*1109C>T| S256
173871 BAA02g16980 A02 8420124 A T downstream_gene_variant MODIFIER c.*656T>A| S153
S213
173872 BAA02g16980 A02 8420369 C T downstream_gene_variant MODIFIER c.*411G>A| S175
173873 BAA02g16980 A02 8421537 G A intron_variant MODIFIER c.774+41C>T| S279
173874 BAA02g16980 A02 8421612 C T missense_variant MODERATE c.740G>A|p.Cys247Tyr S39
173875 BAA02g16980 A02 8422319 C T missense_variant MODERATE c.388G>A|p.Glu130Lys S111