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
198301 BAA02g29680 A02 17028720 G A upstream_gene_variant MODIFIER c.-3169C>T| S148
S30
S31
198302 BAA02g29680 A02 17029592 C T upstream_gene_variant MODIFIER c.-4041G>A| S266
198303 BAA02g29680 A02 17029616 G A upstream_gene_variant MODIFIER c.-4065C>T| S288
198304 BAA02g29690 A02 17032186 G A downstream_gene_variant MODIFIER c.*873C>T| S127
198305 BAA02g29690 A02 17034009 G A synonymous_variant LOW c.606C>T|p.Leu202Leu S191
198306 BAA02g29690 A02 17034103 G A splice_region_variant&intron_variant LOW c.520-8C>T| S281
198307 BAA02g29690 A02 17035571 C T missense_variant MODERATE c.40G>A|p.Glu14Lys S15
198308 BAA02g29690 A02 17036180 G A upstream_gene_variant MODIFIER c.-570C>T| S291
198309 BAA02g29690 A02 17037771 G A upstream_gene_variant MODIFIER c.-2161C>T| S196
198310 BAA02g29690 A02 17037963 G A upstream_gene_variant MODIFIER c.-2353C>T| S5
198311 BAA02g29700 A02 17040058 C T missense_variant MODERATE c.74G>A|p.Gly25Glu S185
198312 BAA02g29700 A02 17040099 C T splice_region_variant&intron_variant LOW c.40-7G>A| S301
S304
198313 BAA02g29690 A02 17040126 C T upstream_gene_variant MODIFIER c.-4516G>A| S262
198314 BAA02g29710 A02 17041225 G A missense_variant MODERATE c.140G>A|p.Gly47Asp S61
198315 BAA02g29700 A02 17042140 C T upstream_gene_variant MODIFIER c.-1928G>A| S231
198316 BAA02g29700 A02 17042301 C T upstream_gene_variant MODIFIER c.-2089G>A| S231
198317 BAA02g29700 A02 17043523 G A upstream_gene_variant MODIFIER c.-3311C>T| S199
198318 BAA02g29700 A02 17044512 C T upstream_gene_variant MODIFIER c.-4300G>A| S167
198319 BAA02g29700 A02 17044812 G A upstream_gene_variant MODIFIER c.-4600C>T| S259
198320 BAA02g29700 A02 17044944 C T upstream_gene_variant MODIFIER c.-4732G>A| S233
198321 BAA02g29700 A02 17045192 C T upstream_gene_variant MODIFIER c.-4980G>A| S107
198322 BAA02g29720 A02 17045407 C T synonymous_variant LOW c.1416G>A|p.Lys472Lys S180
198323 BAA02g29720 A02 17045456 C T missense_variant MODERATE c.1367G>A|p.Ser456Asn S177
198324 BAA02g29720 A02 17045610 G A missense_variant MODERATE c.1213C>T|p.Leu405Phe S205
198325 BAA02g29720 A02 17045616 G A missense_variant&splice_region_variant MODERATE c.1207C>T|p.Pro403Ser S25