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
179101 BAA02g19740 A02 10282052 C T intron_variant MODIFIER c.3189+2024G>A| S275
179102 BAA02g19740 A02 10282360 G A intron_variant MODIFIER c.3189+1716C>T| S265
179103 BAA02g19740 A02 10282533 G A intron_variant MODIFIER c.3189+1543C>T| S210
179104 BAA02g19740 A02 10282566 G A intron_variant MODIFIER c.3189+1510C>T| S245
179105 BAA02g19740 A02 10282601 C T intron_variant MODIFIER c.3189+1475G>A| S166
179106 BAA02g19740 A02 10283466 G A intron_variant MODIFIER c.3189+610C>T| S282
179107 BAA02g19740 A02 10284099 G A missense_variant MODERATE c.3166C>T|p.Pro1056Ser S7
179108 BAA02g19740 A02 10284124 G A synonymous_variant LOW c.3141C>T|p.His1047His S189
179109 BAA02g19740 A02 10284226 C T synonymous_variant LOW c.3039G>A|p.Ala1013Ala S135
179110 BAA02g19740 A02 10284430 G A synonymous_variant LOW c.2835C>T|p.Leu945Leu S193
179111 BAA02g19740 A02 10285019 C T missense_variant MODERATE c.2246G>A|p.Gly749Glu S58
179112 BAA02g19740 A02 10285188 G A missense_variant MODERATE c.2077C>T|p.His693Tyr S303
179113 BAA02g19740 A02 10285762 G A missense_variant MODERATE c.1577C>T|p.Ser526Leu S296
179114 BAA02g19740 A02 10285879 G A missense_variant MODERATE c.1460C>T|p.Ser487Phe S129
179115 BAA02g19740 A02 10286587 C T intron_variant MODIFIER c.833+14G>A| S275
179116 BAA02g19740 A02 10286785 G A missense_variant MODERATE c.649C>T|p.Pro217Ser S282
179117 BAA02g19740 A02 10287070 G A missense_variant MODERATE c.364C>T|p.Pro122Ser S190
179118 BAA02g19740 A02 10287211 G A missense_variant MODERATE c.223C>T|p.Leu75Phe S282
179119 BAA02g19740 A02 10287253 G A missense_variant MODERATE c.181C>T|p.Pro61Ser S240
179120 BAA02g19740 A02 10287434 C T intron_variant MODIFIER c.103+10G>A| S262
179121 BAA02g19740 A02 10288423 C T upstream_gene_variant MODIFIER c.-877G>A| S211
S227
179122 BAA02g19740 A02 10288683 C T upstream_gene_variant MODIFIER c.-1137G>A| S119
179123 BAA02g19740 A02 10289113 C T upstream_gene_variant MODIFIER c.-1567G>A| S183
S198
179124 BAA02g19740 A02 10290154 C T upstream_gene_variant MODIFIER c.-2608G>A| S65
179125 BAA02g19740 A02 10292133 C T upstream_gene_variant MODIFIER c.-4587G>A| S163