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
44151 BAA01g26870 A01 15145234 G A upstream_gene_variant MODIFIER c.-4614G>A| S144
44152 BAA01g26850 A01 15145381 C T synonymous_variant LOW c.2184C>T|p.Ile728Ile S99
44153 BAA01g26870 A01 15146470 G A upstream_gene_variant MODIFIER c.-3378G>A| S294
44154 BAA01g26870 A01 15146700 C T upstream_gene_variant MODIFIER c.-3148C>T| S161
44155 BAA01g26870 A01 15146801 C T upstream_gene_variant MODIFIER c.-3047C>T| S153
44156 BAA01g26860 A01 15148028 C T missense_variant MODERATE c.1444G>A|p.Ala482Thr S25
S259
44157 BAA01g26860 A01 15148112 C T missense_variant MODERATE c.1360G>A|p.Glu454Lys S189
44158 BAA01g26860 A01 15148242 C T synonymous_variant LOW c.1230G>A|p.Lys410Lys S55
44159 BAA01g26860 A01 15148340 C T missense_variant MODERATE c.1132G>A|p.Asp378Asn S20
44160 BAA01g26860 A01 15149701 C T upstream_gene_variant MODIFIER c.-230G>A| S20
44161 BAA01g26880 A01 15152467 C T missense_variant MODERATE c.247G>A|p.Gly83Arg S266
44162 BAA01g26860 A01 15152843 G A upstream_gene_variant MODIFIER c.-3372C>T| S246
44163 BAA01g26860 A01 15153352 G A upstream_gene_variant MODIFIER c.-3881C>T| S202
44164 BAA01g26860 A01 15153588 C T upstream_gene_variant MODIFIER c.-4117G>A| S275
44165 BAA01g26880 A01 15155429 G A upstream_gene_variant MODIFIER c.-2716C>T| S105
S106
44166 BAA01g26880 A01 15155441 C T upstream_gene_variant MODIFIER c.-2728G>A| S113
44167 BAA01g26890 A01 15163090 C T downstream_gene_variant MODIFIER c.*4887G>A| S206
S26
44168 BAA01g26890 A01 15163419 G A downstream_gene_variant MODIFIER c.*4558C>T| S60
44169 BAA01g26890 A01 15163698 G A downstream_gene_variant MODIFIER c.*4279C>T| S124
44170 BAA01g26890 A01 15163803 G A downstream_gene_variant MODIFIER c.*4174C>T| S162
44171 BAA01g26890 A01 15164138 G A downstream_gene_variant MODIFIER c.*3839C>T| S105
S106
44172 BAA01g26890 A01 15164920 G A downstream_gene_variant MODIFIER c.*3057C>T| S84
S93
44173 BAA01g26890 A01 15165134 C T downstream_gene_variant MODIFIER c.*2843G>A| S61
44174 BAA01g26890 A01 15165258 G A downstream_gene_variant MODIFIER c.*2719C>T| S266
44175 BAA01g26890 A01 15165276 C T downstream_gene_variant MODIFIER c.*2701G>A| S25