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
192001 BAA02g26720 A02 14941101 G A downstream_gene_variant MODIFIER c.*4711C>T| S188
192002 BAA02g26720 A02 14941244 G A downstream_gene_variant MODIFIER c.*4568C>T| S246
192003 BAA02g26720 A02 14941444 G A downstream_gene_variant MODIFIER c.*4368C>T| S168
192004 BAA02g26710 A02 14944947 C T downstream_gene_variant MODIFIER c.*3128C>T| S185
192005 BAA02g26710 A02 14945318 C T downstream_gene_variant MODIFIER c.*3499C>T| S308
192006 BAA02g26710 A02 14945526 G A downstream_gene_variant MODIFIER c.*3707G>A| S236
192007 BAA02g26710 A02 14945644 C T downstream_gene_variant MODIFIER c.*3825C>T| S131
192008 BAA02g26720 A02 14947183 G A intron_variant MODIFIER c.510-35C>T| S37
192009 BAA02g26720 A02 14947444 C T missense_variant MODERATE c.373G>A|p.Glu125Lys S157
S163
192010 BAA02g26720 A02 14947978 G A upstream_gene_variant MODIFIER c.-83C>T| S210
S225
192011 BAA02g26720 A02 14948302 G A upstream_gene_variant MODIFIER c.-407C>T| S19
192012 BAA02g26720 A02 14948863 C T upstream_gene_variant MODIFIER c.-968G>A| S226
192013 BAA02g26720 A02 14950685 C T upstream_gene_variant MODIFIER c.-2790G>A| S51
192014 BAA02g26720 A02 14950712 C T upstream_gene_variant MODIFIER c.-2817G>A| S1
S90
192015 BAA02g26720 A02 14952042 G A upstream_gene_variant MODIFIER c.-4147C>T| S155
192016 BAA02g26720 A02 14952400 G A upstream_gene_variant MODIFIER c.-4505C>T| S19
192017 BAA02g26730 A02 14953468 G A intron_variant MODIFIER c.2509+174C>T| S249
192018 BAA02g26730 A02 14953478 G A intron_variant MODIFIER c.2509+164C>T| S155
S211
192019 BAA02g26730 A02 14953993 G A intron_variant MODIFIER c.2298+9C>T| S146
192020 BAA02g26730 A02 14954775 C T missense_variant MODERATE c.1783G>A|p.Glu595Lys S237
192021 BAA02g26730 A02 14954946 G A missense_variant MODERATE c.1697C>T|p.Ala566Val S28
192022 BAA02g26730 A02 14955382 G A intron_variant MODIFIER c.1576+41C>T| S34
192023 BAA02g26730 A02 14955854 G A intron_variant MODIFIER c.1323+13C>T| S148
S210
192024 BAA02g26730 A02 14956129 C T intron_variant MODIFIER c.1233-172G>A| S179
192025 BAA02g26730 A02 14960912 C T missense_variant MODERATE c.577G>A|p.Gly193Arg S278