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
164251 BAA02g10800 A02 4829698 G A upstream_gene_variant MODIFIER c.-591G>A| S19
164252 BAA02g10800 A02 4830055 G A upstream_gene_variant MODIFIER c.-234G>A| S205
164253 BAA02g10800 A02 4830996 G A missense_variant MODERATE c.326G>A|p.Ser109Asn S43
164254 BAA02g10800 A02 4831422 C T missense_variant MODERATE c.547C>T|p.Pro183Ser S183
S198
164255 BAA02g10810 A02 4831682 C T upstream_gene_variant MODIFIER c.-1146C>T| S6
164256 BAA02g10810 A02 4832417 C T upstream_gene_variant MODIFIER c.-411C>T| S85
164257 BAA02g10810 A02 4832698 G A upstream_gene_variant MODIFIER c.-130G>A| S155
S211
164258 BAA02g10810 A02 4832727 C T upstream_gene_variant MODIFIER c.-101C>T| S305
164259 BAA02g10820 A02 4833585 G A upstream_gene_variant MODIFIER c.-2371G>A| S11
164260 BAA02g10820 A02 4834091 C T upstream_gene_variant MODIFIER c.-1865C>T| S204
164261 BAA02g10820 A02 4836274 C T missense_variant MODERATE c.319C>T|p.Arg107Cys S135
164262 BAA02g10820 A02 4837180 C T missense_variant MODERATE c.799C>T|p.Pro267Ser S182
164263 BAA02g10820 A02 4838344 C T missense_variant MODERATE c.1492C>T|p.Pro498Ser S38
164264 BAA02g10830 A02 4838480 C T upstream_gene_variant MODIFIER c.-3551C>T| S100
164265 BAA02g10830 A02 4838507 G A upstream_gene_variant MODIFIER c.-3524G>A| S173
164266 BAA02g10830 A02 4839069 G A upstream_gene_variant MODIFIER c.-2962G>A| S148
S210
S30
S31
164267 BAA02g10830 A02 4839428 G A upstream_gene_variant MODIFIER c.-2603G>A| S148
S210
S30
S31
164268 BAA02g10830 A02 4840338 C T upstream_gene_variant MODIFIER c.-1693C>T| S244
164269 BAA02g10830 A02 4840355 C T upstream_gene_variant MODIFIER c.-1676C>T| S18
164270 BAA02g10840 A02 4844435 C T upstream_gene_variant MODIFIER c.-890C>T| S277
164271 BAA02g10840 A02 4845317 G A upstream_gene_variant MODIFIER c.-8G>A| S298
164272 BAA02g10840 A02 4845834 G A synonymous_variant LOW c.291G>A|p.Lys97Lys S168
164273 BAA02g10850 A02 4847876 C T upstream_gene_variant MODIFIER c.-4452C>T| S181
164274 BAA02g10850 A02 4851514 G A upstream_gene_variant MODIFIER c.-814G>A| S125
164275 BAA02g10850 A02 4852371 G A missense_variant MODERATE c.44G>A|p.Arg15His S177