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
215851 BAA02g32290 A02 27178733 C T upstream_gene_variant MODIFIER c.-2625C>T| S188
215852 BAA02g32290 A02 27180095 G A upstream_gene_variant MODIFIER c.-1263G>A| S148
S210
215853 BAA02g32290 A02 27180104 C T upstream_gene_variant MODIFIER c.-1254C>T| S249
215854 BAA02g32290 A02 27180265 C T upstream_gene_variant MODIFIER c.-1093C>T| S183
S198
215855 BAA02g32290 A02 27180468 G A upstream_gene_variant MODIFIER c.-890G>A| S232
215856 BAA02g32290 A02 27180572 G A upstream_gene_variant MODIFIER c.-786G>A| S267
215857 BAA02g32290 A02 27181612 G A synonymous_variant LOW c.255G>A|p.Leu85Leu S251
215858 BAA02g32290 A02 27181674 C T missense_variant MODERATE c.317C>T|p.Ser106Phe S140
215859 BAA02g32290 A02 27182073 A T missense_variant MODERATE c.716A>T|p.Asn239Ile S34
215860 BAA02g32290 A02 27182645 G A missense_variant MODERATE c.1288G>A|p.Glu430Lys S293
215861 BAA02g32290 A02 27182725 G A synonymous_variant LOW c.1368G>A|p.Ser456Ser S71
215862 BAA02g32290 A02 27182957 G A downstream_gene_variant MODIFIER c.*58G>A| S156
215863 BAA02g32290 A02 27183330 C T downstream_gene_variant MODIFIER c.*431C>T| S201
215864 BAA02g32290 A02 27184442 A T downstream_gene_variant MODIFIER c.*1543A>T| S61
215865 BAA02g32300 A02 27188448 G A downstream_gene_variant MODIFIER c.*3171C>T| S279
215866 BAA02g32300 A02 27188491 G A downstream_gene_variant MODIFIER c.*3128C>T| S34
215867 BAA02g32300 A02 27190927 G A downstream_gene_variant MODIFIER c.*692C>T| S136
S247
215868 BAA02g32300 A02 27191084 C T downstream_gene_variant MODIFIER c.*535G>A| S64
215869 BAA02g32300 A02 27191629 G A missense_variant MODERATE c.3152C>T|p.Thr1051Ile S35
215870 BAA02g32300 A02 27191858 C T missense_variant MODERATE c.2923G>A|p.Glu975Lys S131
215871 BAA02g32300 A02 27192225 C T missense_variant MODERATE c.2635G>A|p.Glu879Lys S231
215872 BAA02g32300 A02 27192363 C T splice_region_variant&synonymous_variant LOW c.2592G>A|p.Leu864Leu S162
215873 BAA02g32300 A02 27192492 G A synonymous_variant LOW c.2463C>T|p.Asp821Asp S95
215874 BAA02g32300 A02 27193232 C T missense_variant MODERATE c.1723G>A|p.Glu575Lys S112
215875 BAA02g32300 A02 27194742 G A intron_variant MODIFIER c.566-26C>T| S159
S243