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
163151 BAA02g09960 A02 4393791 C T upstream_gene_variant MODIFIER c.-4484C>T| S189
163152 BAA02g09960 A02 4395070 C T upstream_gene_variant MODIFIER c.-3205C>T| S135
163153 BAA02g09960 A02 4395858 C T upstream_gene_variant MODIFIER c.-2417C>T| S156
S34
163154 BAA02g09960 A02 4396467 G A upstream_gene_variant MODIFIER c.-1808G>A| S53
163155 BAA02g09960 A02 4396573 G A upstream_gene_variant MODIFIER c.-1702G>A| S282
163156 BAA02g09960 A02 4396852 G A upstream_gene_variant MODIFIER c.-1423G>A| S260
163157 BAA02g09960 A02 4396935 G A upstream_gene_variant MODIFIER c.-1340G>A| S150
163158 BAA02g09960 A02 4397980 C T upstream_gene_variant MODIFIER c.-295C>T| S168
163159 BAA02g09960 A02 4398379 G A stop_gained HIGH c.105G>A|p.Trp35* S187
163160 BAA02g09970 A02 4402023 C T upstream_gene_variant MODIFIER c.-714C>T| S65
163161 BAA02g09970 A02 4402784 G A synonymous_variant LOW c.48G>A|p.Ala16Ala S296
163162 BAA02g09970 A02 4404000 C T missense_variant MODERATE c.499C>T|p.Leu167Phe S182
163163 BAA02g09960 A02 4404705 G A downstream_gene_variant MODIFIER c.*4143G>A| S149
163164 BAA02g09970 A02 4405982 G A missense_variant MODERATE c.1559G>A|p.Gly520Glu S265
163165 BAA02g09970 A02 4406282 G A downstream_gene_variant MODIFIER c.*146G>A| S206
S26
163166 BAA02g09980 A02 4408964 G A upstream_gene_variant MODIFIER c.-4262G>A| S37
163167 BAA02g09980 A02 4413527 T C missense_variant MODERATE c.302T>C|p.Val101Ala S64
163168 BAA02g09990 A02 4415080 C T upstream_gene_variant MODIFIER c.-474C>T| S250
163169 BAA02g09990 A02 4415724 C T synonymous_variant LOW c.171C>T|p.Phe57Phe S209
163170 BAA02g09990 A02 4415827 C T missense_variant MODERATE c.274C>T|p.Pro92Ser S209
163171 BAA02g10000 A02 4416628 C T upstream_gene_variant MODIFIER c.-2010C>T| S15
S3
163172 BAA02g10000 A02 4417756 C T upstream_gene_variant MODIFIER c.-882C>T| S251
163173 BAA02g10000 A02 4418899 C T missense_variant MODERATE c.262C>T|p.Arg88Cys S233
163174 BAA02g10010 A02 4420334 C T splice_region_variant&synonymous_variant LOW c.699G>A|p.Arg233Arg S305
163175 BAA02g09990 A02 4420945 G A downstream_gene_variant MODIFIER c.*4480G>A| S161