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
176901 BAA02g18580-BAA02g18590 A02 9519533 G A intergenic_region MODIFIER n.9519533G>A| S70
176902 BAA02g18590 A02 9519899 C T upstream_gene_variant MODIFIER c.-4674C>T| S233
176903 BAA02g18590 A02 9520169 G A upstream_gene_variant MODIFIER c.-4404G>A| S207
S68
176904 BAA02g18590 A02 9520334 G A upstream_gene_variant MODIFIER c.-4239G>A| S136
176905 BAA02g18590 A02 9520443 G A upstream_gene_variant MODIFIER c.-4130G>A| S146
176906 BAA02g18590 A02 9521889 G A upstream_gene_variant MODIFIER c.-2684G>A| S288
176907 BAA02g18590 A02 9522668 C T upstream_gene_variant MODIFIER c.-1905C>T| S208
S219
176908 BAA02g18590 A02 9522767 C T upstream_gene_variant MODIFIER c.-1806C>T| S224
176909 BAA02g18590 A02 9522996 G A upstream_gene_variant MODIFIER c.-1577G>A| S86
176910 BAA02g18590 A02 9524205 G A upstream_gene_variant MODIFIER c.-368G>A| S296
176911 BAA02g18590 A02 9524669 G A splice_donor_variant&intron_variant HIGH c.96+1G>A| S62
176912 BAA02g18590 A02 9525322 C T intron_variant MODIFIER c.193-187C>T| S130
176913 BAA02g18590 A02 9525502 C T splice_region_variant&intron_variant LOW c.193-7C>T| S123
176914 BAA02g18590 A02 9526055 G A stop_gained HIGH c.452G>A|p.Trp151* S148
S30
S31
176915 BAA02g18590 A02 9526565 G A downstream_gene_variant MODIFIER c.*22G>A| S269
176916 BAA02g18590 A02 9527239 G A downstream_gene_variant MODIFIER c.*696G>A| S132
S137
S215
176917 BAA02g18610 A02 9530219 G A upstream_gene_variant MODIFIER c.-2709G>A| S19
176918 BAA02g18610 A02 9531098 G A upstream_gene_variant MODIFIER c.-1830G>A| S206
S26
176919 BAA02g18600 A02 9531273 C T missense_variant MODERATE c.406G>A|p.Gly136Ser S135
176920 BAA02g18600 A02 9531301 G A synonymous_variant LOW c.378C>T|p.Leu126Leu S191
176921 BAA02g18600 A02 9531478 G A synonymous_variant LOW c.201C>T|p.Leu67Leu S166
176922 BAA02g18600 A02 9531584 C T missense_variant MODERATE c.95G>A|p.Gly32Glu S277
176923 BAA02g18600 A02 9531655 C T splice_region_variant&intron_variant LOW c.27-3G>A| S124
176924 BAA02g18610 A02 9531723 G A upstream_gene_variant MODIFIER c.-1205G>A| S148
176925 BAA02g18610 A02 9531730 G A upstream_gene_variant MODIFIER c.-1198G>A| S170