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
153851 BAA02g02240 A02 1005996 G A upstream_gene_variant MODIFIER c.-3863G>A| S241
153852 BAA02g02230 A02 1007303 G A missense_variant MODERATE c.227C>T|p.Thr76Ile S244
153853 BAA02g02230 A02 1008091 C T upstream_gene_variant MODIFIER c.-562G>A| S133
153854 BAA02g02230 A02 1008209 G A upstream_gene_variant MODIFIER c.-680C>T| S162
153855 BAA02g02230 A02 1008590 C T upstream_gene_variant MODIFIER c.-1061G>A| S183
S228
153856 BAA02g02230 A02 1009050 C T upstream_gene_variant MODIFIER c.-1521G>A| S195
153857 BAA02g02240 A02 1009932 C T missense_variant MODERATE c.74C>T|p.Pro25Leu S230
153858 BAA02g02240 A02 1010055 C T missense_variant MODERATE c.197C>T|p.Ser66Phe S179
153859 BAA02g02240 A02 1010225 C T synonymous_variant LOW c.367C>T|p.Leu123Leu S65
153860 BAA02g02240 A02 1010336 G A missense_variant MODERATE c.478G>A|p.Glu160Lys S188
153861 BAA02g02240 A02 1010586 G A missense_variant MODERATE c.728G>A|p.Gly243Asp S203
153862 BAA02g02240 A02 1010678 C T missense_variant MODERATE c.820C>T|p.Pro274Ser S71
153863 BAA02g02240 A02 1010927 G A missense_variant MODERATE c.1069G>A|p.Val357Met S279
153864 BAA02g02240 A02 1011911 C T missense_variant MODERATE c.2053C>T|p.His685Tyr S117
153865 BAA02g02240 A02 1012347 C T synonymous_variant LOW c.2421C>T|p.Phe807Phe S18
153866 BAA02g02250 A02 1012704 C T upstream_gene_variant MODIFIER c.-1427C>T| S211
S227
153867 BAA02g02250 A02 1013078 G A upstream_gene_variant MODIFIER c.-1053G>A| S305
153868 BAA02g02250 A02 1013194 G A upstream_gene_variant MODIFIER c.-937G>A| S205
153869 BAA02g02250 A02 1014685 G A stop_gained HIGH c.555G>A|p.Trp185* S87
153870 BAA02g02250 A02 1015468 G A missense_variant MODERATE c.961G>A|p.Gly321Arg S107
153871 BAA02g02250 A02 1015757 G A stop_gained HIGH c.1172G>A|p.Trp391* S23
153872 BAA02g02250 A02 1016217 G A missense_variant MODERATE c.1436G>A|p.Arg479Lys S202
153873 BAA02g02240 A02 1017069 T G downstream_gene_variant MODIFIER c.*4662T>G| S18
153874 BAA02g02240 A02 1017123 G A downstream_gene_variant MODIFIER c.*4716G>A| S172
S202
S217
153875 BAA02g02240 A02 1017125 G A downstream_gene_variant MODIFIER c.*4718G>A| S11