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
194101 BAA02g27790 A02 15631844 C T upstream_gene_variant MODIFIER c.-88G>A| S131
194102 BAA02g27790 A02 15632731 G A upstream_gene_variant MODIFIER c.-975C>T| S71
194103 BAA02g27790 A02 15634518 C T upstream_gene_variant MODIFIER c.-2762G>A| S273
194104 BAA02g27790 A02 15635537 G A upstream_gene_variant MODIFIER c.-3781C>T| S57
194105 BAA02g27800 A02 15637072 C T intron_variant MODIFIER c.741+868C>T| S54
194106 BAA02g27800 A02 15637324 G A intron_variant MODIFIER c.742-737G>A| S209
194107 BAA02g27800 A02 15637565 G A intron_variant MODIFIER c.742-496G>A| S238
194108 BAA02g27800 A02 15638247 C T intron_variant MODIFIER c.870+58C>T| S178
194109 BAA02g27800 A02 15638984 G A intron_variant MODIFIER c.1247+198G>A| S217
194110 BAA02g27800 A02 15639015 G A intron_variant MODIFIER c.1247+229G>A| S256
194111 BAA02g27800 A02 15639684 C T missense_variant MODERATE c.1646C>T|p.Ser549Phe S109
194112 BAA02g27800 A02 15639844 G A intron_variant MODIFIER c.1750+56G>A| S82
S92
194113 BAA02g27800 A02 15640041 C T intron_variant MODIFIER c.1750+253C>T| S140
194114 BAA02g27800 A02 15640374 C T intron_variant MODIFIER c.1751-161C>T| S286
194115 BAA02g27800 A02 15641009 G A missense_variant MODERATE c.2225G>A|p.Arg742Lys S281
194116 BAA02g27800 A02 15642335 G A downstream_gene_variant MODIFIER c.*836G>A| S261
194117 BAA02g27800 A02 15642421 C T downstream_gene_variant MODIFIER c.*922C>T| S171
194118 BAA02g27800 A02 15642473 G A downstream_gene_variant MODIFIER c.*974G>A| S281
194119 BAA02g27800 A02 15642538 G A downstream_gene_variant MODIFIER c.*1039G>A| S41
194120 BAA02g27800 A02 15643325 G A downstream_gene_variant MODIFIER c.*1826G>A| S98
194121 BAA02g27800 A02 15643349 G A downstream_gene_variant MODIFIER c.*1850G>A| S113
194122 BAA02g27800 A02 15643433 G A downstream_gene_variant MODIFIER c.*1934G>A| S232
194123 BAA02g27800 A02 15643708 C T downstream_gene_variant MODIFIER c.*2209C>T| S177
194124 BAA02g27800 A02 15644258 G A downstream_gene_variant MODIFIER c.*2759G>A| S203
194125 BAA02g27800 A02 15644785 G A downstream_gene_variant MODIFIER c.*3286G>A| S167
S210
S225