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
219051 BAA02g33110 A02 28357260 G A upstream_gene_variant MODIFIER c.-4222G>A| S297
219052 BAA02g33110 A02 28358722 C A upstream_gene_variant MODIFIER c.-2760C>A| S268
219053 BAA02g33110 A02 28359425 C T upstream_gene_variant MODIFIER c.-2057C>T| S177
219054 BAA02g33110 A02 28361047 C T upstream_gene_variant MODIFIER c.-435C>T| S112
219055 BAA02g33110 A02 28361446 G A upstream_gene_variant MODIFIER c.-36G>A| S13
219056 BAA02g33110 A02 28361659 G A missense_variant MODERATE c.178G>A|p.Ala60Thr S217
219057 BAA02g33110 A02 28361763 G A synonymous_variant LOW c.282G>A|p.Leu94Leu S59
219058 BAA02g33110 A02 28362001 C T missense_variant MODERATE c.520C>T|p.Pro174Ser S274
219059 BAA02g33110 A02 28363186 C T intron_variant MODIFIER c.781-66C>T| S144
219060 BAA02g33110 A02 28363363 G A missense_variant MODERATE c.892G>A|p.Gly298Arg S223
219061 BAA02g33110 A02 28363364 G A missense_variant MODERATE c.893G>A|p.Gly298Glu S207
219062 BAA02g33110 A02 28363479 C T synonymous_variant LOW c.1008C>T|p.Tyr336Tyr S206
219063 BAA02g33110 A02 28363526 C T missense_variant MODERATE c.1055C>T|p.Ser352Phe S75
S81
219064 BAA02g33110 A02 28363772 C T missense_variant MODERATE c.1301C>T|p.Ser434Phe S65
219065 BAA02g33110 A02 28363829 G A missense_variant MODERATE c.1358G>A|p.Ser453Asn S35
219066 BAA02g33110 A02 28364477 G A downstream_gene_variant MODIFIER c.*425G>A| S47
219067 BAA02g33110 A02 28364515 G A downstream_gene_variant MODIFIER c.*463G>A| S7
219068 BAA02g33110 A02 28364576 C T downstream_gene_variant MODIFIER c.*524C>T| S262
219069 BAA02g33110 A02 28364682 C T downstream_gene_variant MODIFIER c.*630C>T| S175
S177
219070 BAA02g33110 A02 28365316 G A downstream_gene_variant MODIFIER c.*1264G>A| S132
S137
S215
S89
219071 BAA02g33110 A02 28365831 C T downstream_gene_variant MODIFIER c.*1779C>T| S15
219072 BAA02g33110 A02 28365949 C T downstream_gene_variant MODIFIER c.*1897C>T| S138
219073 BAA02g33110 A02 28366019 C T downstream_gene_variant MODIFIER c.*1967C>T| S100
219074 BAA02g33110-BAA02g33120 A02 28369318 G A intergenic_region MODIFIER n.28369318G>A| S156
219075 BAA02g33110-BAA02g33120 A02 28371237 C T intergenic_region MODIFIER n.28371237C>T| S54