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
174201 BAA02g17140 A02 8542670 G A synonymous_variant LOW c.153C>T|p.Ser51Ser S157
174202 BAA02g17140 A02 8543368 C T upstream_gene_variant MODIFIER c.-468G>A| S12
174203 BAA02g17140 A02 8546092 C T upstream_gene_variant MODIFIER c.-3192G>A| S163
174204 BAA02g17160 A02 8547158 C T synonymous_variant LOW c.96C>T|p.Leu32Leu S282
174205 BAA02g17160 A02 8547159 C T missense_variant MODERATE c.97C>T|p.Pro33Ser S34
174206 BAA02g17160 A02 8548191 G A synonymous_variant LOW c.1041G>A|p.Val347Val S197
174207 BAA02g17160 A02 8548345 G A missense_variant MODERATE c.1195G>A|p.Glu399Lys S202
174208 BAA02g17160 A02 8548506 G A synonymous_variant LOW c.1356G>A|p.Gly452Gly S4
174209 BAA02g17160 A02 8549130 C T missense_variant MODERATE c.1789C>T|p.His597Tyr S127
174210 BAA02g17160 A02 8549203 C T missense_variant MODERATE c.1862C>T|p.Ser621Phe S255
174211 BAA02g17160 A02 8549232 C T missense_variant MODERATE c.1891C>T|p.Arg631Cys S18
174212 BAA02g17160 A02 8549318 C T synonymous_variant LOW c.1977C>T|p.Leu659Leu S223
174213 BAA02g17160 A02 8549361 C T missense_variant MODERATE c.2020C>T|p.Pro674Ser S302
174214 BAA02g17160 A02 8550533 C T synonymous_variant LOW c.2838C>T|p.Leu946Leu S194
174215 BAA02g17160 A02 8550783 G A missense_variant MODERATE c.3088G>A|p.Asp1030Asn S69
174216 BAA02g17170 A02 8550946 C T upstream_gene_variant MODIFIER c.-439C>T| S255
174217 BAA02g17160 A02 8552085 G A downstream_gene_variant MODIFIER c.*1174G>A| S289
S290
174218 BAA02g17160 A02 8552365 G A downstream_gene_variant MODIFIER c.*1454G>A| S136
174219 BAA02g17180 A02 8553767 G A synonymous_variant LOW c.1738C>T|p.Leu580Leu S155
174220 BAA02g17180 A02 8554543 C T missense_variant MODERATE c.962G>A|p.Gly321Asp S171
174221 BAA02g17180 A02 8555280 G A synonymous_variant LOW c.225C>T|p.Thr75Thr S274
174222 BAA02g17180 A02 8556166 G A upstream_gene_variant MODIFIER c.-662C>T| S111
174223 BAA02g17180 A02 8556206 C T upstream_gene_variant MODIFIER c.-702G>A| S100
174224 BAA02g17180 A02 8556563 G A upstream_gene_variant MODIFIER c.-1059C>T| S170
S197
174225 BAA02g17180 A02 8556602 C T upstream_gene_variant MODIFIER c.-1098G>A| S180