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
76151 BAA01g40080-BAA01g40090 A01 26672145 T A intergenic_region MODIFIER n.26672145T>A| S131
76152 BAA01g40080-BAA01g40090 A01 26672374 G A intergenic_region MODIFIER n.26672374G>A| S271
76153 BAA01g40080-BAA01g40090 A01 26672759 C T intergenic_region MODIFIER n.26672759C>T| S159
S243
76154 BAA01g40080-BAA01g40090 A01 26672771 C T intergenic_region MODIFIER n.26672771C>T| S293
76155 BAA01g40080-BAA01g40090 A01 26673207 G A intergenic_region MODIFIER n.26673207G>A| S265
76156 BAA01g40080-BAA01g40090 A01 26673993 G A intergenic_region MODIFIER n.26673993G>A| S20
76157 BAA01g40080-BAA01g40090 A01 26674106 C T intergenic_region MODIFIER n.26674106C>T| S242
76158 BAA01g40080-BAA01g40090 A01 26676177 G A intergenic_region MODIFIER n.26676177G>A| S60
76159 BAA01g40090 A01 26678714 G A upstream_gene_variant MODIFIER c.-2839G>A| S286
76160 BAA01g40090 A01 26678877 G A upstream_gene_variant MODIFIER c.-2676G>A| S261
76161 BAA01g40090 A01 26679117 C T upstream_gene_variant MODIFIER c.-2436C>T| S256
76162 BAA01g40090 A01 26680331 C T upstream_gene_variant MODIFIER c.-1222C>T| S177
76163 BAA01g40090 A01 26680360 G A upstream_gene_variant MODIFIER c.-1193G>A| S84
S93
76164 BAA01g40090 A01 26680985 C T upstream_gene_variant MODIFIER c.-568C>T| S19
76165 BAA01g40090 A01 26681604 G A missense_variant MODERATE c.52G>A|p.Glu18Lys S213
76166 BAA01g40090 A01 26681842 G A splice_region_variant&synonymous_variant LOW c.111G>A|p.Gln37Gln S5
76167 BAA01g40100 A01 26682271 G A upstream_gene_variant MODIFIER c.-4419G>A| S13
76168 BAA01g40090 A01 26683181 C T synonymous_variant LOW c.795C>T|p.Thr265Thr S127
76169 BAA01g40100 A01 26683889 C T upstream_gene_variant MODIFIER c.-2801C>T| S279
76170 BAA01g40100 A01 26684276 G A upstream_gene_variant MODIFIER c.-2414G>A| S70
76171 BAA01g40100 A01 26684966 G A upstream_gene_variant MODIFIER c.-1724G>A| S67
76172 BAA01g40100 A01 26685402 C T upstream_gene_variant MODIFIER c.-1288C>T| S142
76173 BAA01g40100 A01 26686206 C T upstream_gene_variant MODIFIER c.-484C>T| S202
76174 BAA01g40100 A01 26686801 C T missense_variant MODERATE c.112C>T|p.Leu38Phe S164
76175 BAA01g40090 A01 26687049 A G downstream_gene_variant MODIFIER c.*3626A>G| S165
S211
S227