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
126851 BAA10g15510 A10 15831882 G A upstream_gene_variant MODIFIER c.-1894G>A| S278
126852 BAA10g15510 A10 15832792 C T upstream_gene_variant MODIFIER c.-984C>T| S196
126853 BAA10g15510 A10 15833703 C T upstream_gene_variant MODIFIER c.-73C>T| S168
126854 BAA10g15510 A10 15833825 C T missense_variant MODERATE c.50C>T|p.Ala17Val S161
126855 BAA10g15510 A10 15833851 C T stop_gained HIGH c.76C>T|p.Gln26* S169
126856 BAA10g15510 A10 15833861 C T missense_variant MODERATE c.86C>T|p.Ser29Phe S281
126857 BAA10g15510 A10 15834000 C T synonymous_variant LOW c.225C>T|p.Ala75Ala S266
126858 BAA10g15510 A10 15835333 G A downstream_gene_variant MODIFIER c.*424G>A| S164
126859 BAA10g15510 A10 15835437 C T downstream_gene_variant MODIFIER c.*528C>T| S225
126860 BAA10g15510 A10 15835626 C T downstream_gene_variant MODIFIER c.*717C>T| S97
126861 BAA10g15510 A10 15838596 G A downstream_gene_variant MODIFIER c.*3687G>A| S81
126862 BAA10g15510 A10 15838619 G A downstream_gene_variant MODIFIER c.*3710G>A| S288
126863 BAA10g15510 A10 15838901 C T downstream_gene_variant MODIFIER c.*3992C>T| S45
126864 BAA10g15510 A10 15838909 C T downstream_gene_variant MODIFIER c.*4000C>T| S143
126865 BAA10g15520 A10 15841493 C T downstream_gene_variant MODIFIER c.*1271G>A| S73
S91
126866 BAA10g15520 A10 15842634 C T downstream_gene_variant MODIFIER c.*130G>A| S108
126867 BAA10g15520 A10 15842691 C T downstream_gene_variant MODIFIER c.*73G>A| S174
126868 BAA10g15520 A10 15845945 C T upstream_gene_variant MODIFIER c.-339G>A| S20
126869 BAA10g15520 A10 15846083 G A upstream_gene_variant MODIFIER c.-477C>T| S109
126870 BAA10g15520 A10 15849277 G A upstream_gene_variant MODIFIER c.-3671C>T| S262
126871 BAA10g15520 A10 15850362 C T upstream_gene_variant MODIFIER c.-4756G>A| S10
126872 BAA10g15520 A10 15850394 C T upstream_gene_variant MODIFIER c.-4788G>A| S51
126873 BAA10g15530 A10 15850910 G A intron_variant MODIFIER c.544-320C>T| S213
126874 BAA10g15530 A10 15853095 C T missense_variant MODERATE c.490G>A|p.Glu164Lys S283
126875 BAA10g15540 A10 15854662 G A upstream_gene_variant MODIFIER c.-2146G>A| S25