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
81251 BAA01g42980 A01 28450560 G A missense_variant MODERATE c.373G>A|p.Glu125Lys S297
81252 BAA01g42980 A01 28451002 C T downstream_gene_variant MODIFIER c.*134C>T| S23
81253 BAA01g42980 A01 28451137 C T downstream_gene_variant MODIFIER c.*269C>T| S288
81254 BAA01g42980 A01 28451371 G A downstream_gene_variant MODIFIER c.*503G>A| S262
81255 BAA01g42980 A01 28452784 G A downstream_gene_variant MODIFIER c.*1916G>A| S105
S106
81256 BAA01g42980 A01 28453684 G A downstream_gene_variant MODIFIER c.*2816G>A| S244
81257 BAA01g42980 A01 28455104 G A downstream_gene_variant MODIFIER c.*4236G>A| S80
81258 BAA01g42990 A01 28457168 C T upstream_gene_variant MODIFIER c.-4961C>T| S134
81259 BAA01g42990 A01 28458559 G A upstream_gene_variant MODIFIER c.-3570G>A| S85
81260 BAA01g42990 A01 28459017 C T upstream_gene_variant MODIFIER c.-3112C>T| S77
81261 BAA01g42990 A01 28459885 T A upstream_gene_variant MODIFIER c.-2244T>A| S166
81262 BAA01g42990 A01 28459969 G A upstream_gene_variant MODIFIER c.-2160G>A| S208
S219
81263 BAA01g42990 A01 28460866 C T upstream_gene_variant MODIFIER c.-1263C>T| S260
81264 BAA01g42990 A01 28460899 C T upstream_gene_variant MODIFIER c.-1230C>T| S62
81265 BAA01g42990 A01 28461433 C T upstream_gene_variant MODIFIER c.-696C>T| S44
81266 BAA01g43000 A01 28462442 G A downstream_gene_variant MODIFIER c.*4015C>T| S125
81267 BAA01g43000 A01 28462578 C T downstream_gene_variant MODIFIER c.*3879G>A| S205
81268 BAA01g43000 A01 28463213 G A downstream_gene_variant MODIFIER c.*3244C>T| S115
81269 BAA01g42990 A01 28464520 G A splice_donor_variant&intron_variant HIGH c.1155+1G>A| S1
S90
81270 BAA01g42990 A01 28464652 C T missense_variant MODERATE c.1201C>T|p.Leu401Phe S51
S52
81271 BAA01g42990 A01 28464874 G A missense_variant MODERATE c.1279G>A|p.Ala427Thr S108
81272 BAA01g42990 A01 28465455 G A downstream_gene_variant MODIFIER c.*207G>A| S268
81273 BAA01g43000 A01 28466681 C T missense_variant MODERATE c.493G>A|p.Glu165Lys S162
81274 BAA01g43000 A01 28466813 C T missense_variant MODERATE c.361G>A|p.Ala121Thr S158
81275 BAA01g43000 A01 28468177 G A upstream_gene_variant MODIFIER c.-526C>T| S287