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
176051 BAA02g18160 A02 9159820 C T upstream_gene_variant MODIFIER c.-4856G>A| S158
176052 BAA02g18170 A02 9160120 G A upstream_gene_variant MODIFIER c.-3533C>T| S217
S248
176053 BAA02g18170 A02 9160126 G A upstream_gene_variant MODIFIER c.-3539C>T| S92
176054 BAA02g18170 A02 9160274 C T upstream_gene_variant MODIFIER c.-3687G>A| S301
S304
176055 BAA02g18170 A02 9160298 G A upstream_gene_variant MODIFIER c.-3711C>T| S134
176056 BAA02g18170 A02 9160364 C T upstream_gene_variant MODIFIER c.-3777G>A| S180
176057 BAA02g18170 A02 9161095 C T upstream_gene_variant MODIFIER c.-4508G>A| S32
176058 BAA02g18190 A02 9162214 G A synonymous_variant LOW c.87G>A|p.Glu29Glu S188
176059 BAA02g18190 A02 9162256 C T synonymous_variant LOW c.129C>T|p.Asp43Asp S299
176060 BAA02g18190 A02 9163421 C T splice_region_variant&intron_variant LOW c.1212+7C>T| S163
176061 BAA02g18190 A02 9163686 C T missense_variant MODERATE c.1412C>T|p.Ser471Phe S64
176062 BAA02g18190 A02 9163910 C T missense_variant MODERATE c.1636C>T|p.Leu546Phe S158
176063 BAA02g18190 A02 9164078 G A missense_variant MODERATE c.1804G>A|p.Gly602Ser S274
176064 BAA02g18200 A02 9165545 G A upstream_gene_variant MODIFIER c.-1297G>A| S188
176065 BAA02g18200 A02 9167143 G A missense_variant MODERATE c.302G>A|p.Gly101Asp S192
176066 BAA02g18200 A02 9167733 C T missense_variant MODERATE c.892C>T|p.Leu298Phe S5
176067 BAA02g18200 A02 9167806 G A missense_variant MODERATE c.965G>A|p.Arg322Lys S237
176068 BAA02g18200 A02 9167817 G A missense_variant MODERATE c.976G>A|p.Ala326Thr S276
176069 BAA02g18200 A02 9167931 G A missense_variant MODERATE c.1090G>A|p.Glu364Lys S162
176070 BAA02g18200 A02 9169360 G A downstream_gene_variant MODIFIER c.*917G>A| S69
176071 BAA02g18200 A02 9169679 G A downstream_gene_variant MODIFIER c.*1236G>A| S52
176072 BAA02g18200 A02 9171045 C T downstream_gene_variant MODIFIER c.*2602C>T| S202
176073 BAA02g18200 A02 9171834 C T downstream_gene_variant MODIFIER c.*3391C>T| S104
176074 BAA02g18200-BAA02g18210 A02 9173543 G A intergenic_region MODIFIER n.9173543G>A| S295
176075 BAA02g18210 A02 9174934 G A upstream_gene_variant MODIFIER c.-4573G>A| S296