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
13851 BAA01g10790 A01 4980518 C T upstream_gene_variant MODIFIER c.-3954G>A| S42
13852 BAA01g10790 A01 4980900 C T upstream_gene_variant MODIFIER c.-4336G>A| S182
13853 BAA01g10800 A01 4982067 C T upstream_gene_variant MODIFIER c.-4146G>A| S143
13854 BAA01g10820 A01 4982711 T C missense_variant MODERATE c.361A>G|p.Ile121Val S184
13855 BAA01g10810 A01 4983179 C T upstream_gene_variant MODIFIER c.-1808G>A| S242
13856 BAA01g10810 A01 4985002 C T upstream_gene_variant MODIFIER c.-3631G>A| S198
13857 BAA01g10820 A01 4987900 G A upstream_gene_variant MODIFIER c.-4829C>T| S294
13858 BAA01g10830 A01 4988252 C T upstream_gene_variant MODIFIER c.-1337G>A| S176
13859 BAA01g10830 A01 4988259 G A upstream_gene_variant MODIFIER c.-1344C>T| S28
13860 BAA01g10840 A01 4989218 C T missense_variant MODERATE c.2005G>A|p.Gly669Arg S25
S264
13861 BAA01g10840 A01 4989949 C T synonymous_variant LOW c.1419G>A|p.Glu473Glu S282
13862 BAA01g10840 A01 4990038 G A missense_variant MODERATE c.1330C>T|p.Pro444Ser S63
13863 BAA01g10840 A01 4990447 G A synonymous_variant LOW c.1086C>T|p.Leu362Leu S142
13864 BAA01g10840 A01 4991701 C T missense_variant MODERATE c.259G>A|p.Glu87Lys S62
13865 BAA01g10840 A01 4991864 G A synonymous_variant LOW c.96C>T|p.Val32Val S236
13866 BAA01g10840 A01 4992321 G A upstream_gene_variant MODIFIER c.-362C>T| S159
S243
13867 BAA01g10840 A01 4992691 C T upstream_gene_variant MODIFIER c.-732G>A| S179
13868 BAA01g10840 A01 4993150 G C upstream_gene_variant MODIFIER c.-1191C>G| S89
13869 BAA01g10840 A01 4995004 C T upstream_gene_variant MODIFIER c.-3045G>A| S182
13870 BAA01g10840 A01 4995156 G A upstream_gene_variant MODIFIER c.-3197C>T| S3
13871 BAA01g10840 A01 4995455 C T upstream_gene_variant MODIFIER c.-3496G>A| S270
13872 BAA01g10840 A01 4996490 G A upstream_gene_variant MODIFIER c.-4531C>T| S86
13873 BAA01g10840-BAA01g10850 A01 4997893 C T intergenic_region MODIFIER n.4997893C>T| S18
13874 BAA01g10850 A01 5003456 C T upstream_gene_variant MODIFIER c.-126C>T| S166
13875 BAA01g10850 A01 5003629 C T synonymous_variant LOW c.48C>T|p.Thr16Thr S112