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
201801 BAA02g30910 A02 18242920 G A upstream_gene_variant MODIFIER c.-1866C>T| S236
201802 BAA02g30910 A02 18243294 G A upstream_gene_variant MODIFIER c.-2240C>T| S225
S73
201803 BAA02g30910 A02 18243452 G A upstream_gene_variant MODIFIER c.-2398C>T| S61
201804 BAA02g30910 A02 18243478 C T upstream_gene_variant MODIFIER c.-2424G>A| S162
201805 BAA02g30910 A02 18243917 G A upstream_gene_variant MODIFIER c.-2863C>T| S126
201806 BAA02g30920 A02 18244647 C T synonymous_variant LOW c.546G>A|p.Gln182Gln S275
201807 BAA02g30920 A02 18246491 G A upstream_gene_variant MODIFIER c.-1203C>T| S155
S211
201808 BAA02g30920 A02 18247494 C T upstream_gene_variant MODIFIER c.-2206G>A| S251
201809 BAA02g30920 A02 18247767 G A upstream_gene_variant MODIFIER c.-2479C>T| S251
201810 BAA02g30920 A02 18248549 G A upstream_gene_variant MODIFIER c.-3261C>T| S190
201811 BAA02g30920 A02 18249411 G A upstream_gene_variant MODIFIER c.-4123C>T| S191
201812 BAA02g30920 A02 18249756 G A upstream_gene_variant MODIFIER c.-4468C>T| S33
201813 BAA02g30940 A02 18250987 C T downstream_gene_variant MODIFIER c.*720C>T| S49
201814 BAA02g30940 A02 18252318 C T downstream_gene_variant MODIFIER c.*2051C>T| S226
201815 BAA02g30940 A02 18254461 G A downstream_gene_variant MODIFIER c.*4194G>A| S158
201816 BAA02g30950 A02 18256097 C T downstream_gene_variant MODIFIER c.*377G>A| S54
201817 BAA02g30950 A02 18257263 G A intron_variant MODIFIER c.1501+42C>T| S156
201818 BAA02g30950 A02 18257364 C T missense_variant MODERATE c.1442G>A|p.Gly481Glu S183
S198
201819 BAA02g30950 A02 18257713 C T synonymous_variant LOW c.1167G>A|p.Arg389Arg S226
201820 BAA02g30950 A02 18258701 C T intron_variant MODIFIER c.628-39G>A| S140
201821 BAA02g30950 A02 18258803 C T splice_region_variant&intron_variant LOW c.627+4G>A| S40
S49
201822 BAA02g30950 A02 18259644 C T stop_gained HIGH c.236G>A|p.Trp79* S157
S163
201823 BAA02g30950 A02 18259871 G A intron_variant MODIFIER c.156-54C>T| S228
201824 BAA02g30950 A02 18260044 C T intron_variant MODIFIER c.155+79G>A| S75
S81
201825 BAA02g30950 A02 18260123 C T missense_variant&splice_region_variant MODERATE c.155G>A|p.Arg52His S25