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
167901 BAA02g13450 A02 6175821 G A upstream_gene_variant MODIFIER c.-1797G>A| S161
167902 BAA02g13450 A02 6176495 G A upstream_gene_variant MODIFIER c.-1123G>A| S295
167903 BAA02g13450 A02 6176692 C T upstream_gene_variant MODIFIER c.-926C>T| S192
167904 BAA02g13450 A02 6177350 G A upstream_gene_variant MODIFIER c.-268G>A| S45
167905 BAA02g13450 A02 6177851 G A missense_variant MODERATE c.148G>A|p.Ala50Thr S193
167906 BAA02g13450 A02 6178128 C T intron_variant MODIFIER c.298+21C>T| S172
S217
167907 BAA02g13450 A02 6178505 G A missense_variant MODERATE c.538G>A|p.Gly180Arg S48
167908 BAA02g13450 A02 6178735 C T intron_variant MODIFIER c.636+39C>T| S152
167909 BAA02g13450 A02 6179541 C T intron_variant MODIFIER c.1014+57C>T| S185
167910 BAA02g13450 A02 6179952 G A splice_acceptor_variant&intron_variant HIGH c.1182-1G>A| S239
167911 BAA02g13450 A02 6179977 C T synonymous_variant LOW c.1206C>T|p.Asp402Asp S283
167912 BAA02g13450 A02 6180101 G A intron_variant MODIFIER c.1290+40G>A| S166
167913 BAA02g13450 A02 6180228 C T intron_variant MODIFIER c.1346+16C>T| S186
167914 BAA02g13450 A02 6180630 G A intron_variant MODIFIER c.1473+48G>A| S167
S236
S262
S263
167915 BAA02g13450 A02 6180906 C T intron_variant MODIFIER c.1600-27C>T| S165
167916 BAA02g13450 A02 6182344 G A missense_variant MODERATE c.2255G>A|p.Ser752Asn S298
167917 BAA02g13450 A02 6182775 G A missense_variant MODERATE c.2422G>A|p.Glu808Lys S60
167918 BAA02g13450 A02 6184064 C T missense_variant MODERATE c.3137C>T|p.Pro1046Leu S167
167919 BAA02g13450 A02 6185891 C T downstream_gene_variant MODIFIER c.*1644C>T| S115
167920 BAA02g13450 A02 6186494 C T downstream_gene_variant MODIFIER c.*2247C>T| S292
167921 BAA02g13460 A02 6190537 C T downstream_gene_variant MODIFIER c.*128G>A| S174
167922 BAA02g13460 A02 6190590 G A downstream_gene_variant MODIFIER c.*75C>T| S92
167923 BAA02g13460 A02 6190672 C T missense_variant MODERATE c.1979G>A|p.Gly660Asp S245
167924 BAA02g13460 A02 6191675 C T missense_variant MODERATE c.1529G>A|p.Arg510Lys S261
167925 BAA02g13460 A02 6191709 C T missense_variant MODERATE c.1495G>A|p.Val499Met S199