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
197801 BAA02g29440 A02 16856968 G A intron_variant MODIFIER c.69+46C>T| S217
197802 BAA02g29440 A02 16857310 C T upstream_gene_variant MODIFIER c.-228G>A| S18
197803 BAA02g29440 A02 16857869 C T upstream_gene_variant MODIFIER c.-787G>A| S299
197804 BAA02g29440 A02 16857888 C T upstream_gene_variant MODIFIER c.-806G>A| S9
197805 BAA02g29440 A02 16858079 C T upstream_gene_variant MODIFIER c.-997G>A| S242
197806 BAA02g29440 A02 16859422 C T upstream_gene_variant MODIFIER c.-2340G>A| S301
S304
197807 BAA02g29440 A02 16860422 G A upstream_gene_variant MODIFIER c.-3340C>T| S288
197808 BAA02g29440 A02 16861235 G A upstream_gene_variant MODIFIER c.-4153C>T| S263
197809 BAA02g29440 A02 16861617 G A upstream_gene_variant MODIFIER c.-4535C>T| S23
197810 BAA02g29440 A02 16862052 C T upstream_gene_variant MODIFIER c.-4970G>A| S195
197811 BAA02g29450 A02 16862093 C T upstream_gene_variant MODIFIER c.-3758C>T| S126
197812 BAA02g29450 A02 16862293 G A upstream_gene_variant MODIFIER c.-3558G>A| S187
197813 BAA02g29450 A02 16863397 C T upstream_gene_variant MODIFIER c.-2454C>T| S67
197814 BAA02g29450 A02 16863707 C T upstream_gene_variant MODIFIER c.-2144C>T| S139
197815 BAA02g29450 A02 16864641 C T upstream_gene_variant MODIFIER c.-1210C>T| S67
197816 BAA02g29450 A02 16865672 C T upstream_gene_variant MODIFIER c.-179C>T| S219
S72
197817 BAA02g29460 A02 16867617 G A downstream_gene_variant MODIFIER c.*3391C>T| S50
197818 BAA02g29450 A02 16867917 G A missense_variant MODERATE c.541G>A|p.Asp181Asn S249
197819 BAA02g29460 A02 16867994 G A downstream_gene_variant MODIFIER c.*3014C>T| S68
197820 BAA02g29450 A02 16868882 C T downstream_gene_variant MODIFIER c.*777C>T| S294
197821 BAA02g29450 A02 16869578 G A downstream_gene_variant MODIFIER c.*1473G>A| S95
197822 BAA02g29450 A02 16870323 G A downstream_gene_variant MODIFIER c.*2218G>A| S43
197823 BAA02g29460 A02 16871367 G A missense_variant MODERATE c.856C>T|p.Pro286Ser S41
197824 BAA02g29460 A02 16871475 G A missense_variant MODERATE c.748C>T|p.Leu250Phe S263
197825 BAA02g29450 A02 16872913 G A downstream_gene_variant MODIFIER c.*4808G>A| S186