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
43951 BAA01g26790 A01 15078018 G A downstream_gene_variant MODIFIER c.*1003G>A| S105
S229
43952 BAA01g26790 A01 15078035 C T downstream_gene_variant MODIFIER c.*1020C>T| S218
43953 BAA01g26790 A01 15078293 G A downstream_gene_variant MODIFIER c.*1278G>A| S15
S2
S3
S34
S4
S6
43954 BAA01g26790 A01 15078493 G A downstream_gene_variant MODIFIER c.*1478G>A| S181
43955 BAA01g26790 A01 15078843 G A downstream_gene_variant MODIFIER c.*1828G>A| S98
43956 BAA01g26790 A01 15079742 G A downstream_gene_variant MODIFIER c.*2727G>A| S178
43957 BAA01g26790 A01 15080040 C T downstream_gene_variant MODIFIER c.*3025C>T| S20
43958 BAA01g26790 A01 15080383 C T downstream_gene_variant MODIFIER c.*3368C>T| S186
43959 BAA01g26790 A01 15080625 G A downstream_gene_variant MODIFIER c.*3610G>A| S236
43960 BAA01g26790 A01 15081182 C T downstream_gene_variant MODIFIER c.*4167C>T| S112
43961 BAA01g26790 A01 15081574 C T downstream_gene_variant MODIFIER c.*4559C>T| S249
43962 BAA01g26790-BAA01g26800 A01 15083342 C T intergenic_region MODIFIER n.15083342C>T| S20
43963 BAA01g26790-BAA01g26800 A01 15083560 C T intergenic_region MODIFIER n.15083560C>T| S213
43964 BAA01g26790-BAA01g26800 A01 15084481 G A intergenic_region MODIFIER n.15084481G>A| S195
43965 BAA01g26790-BAA01g26800 A01 15084543 G A intergenic_region MODIFIER n.15084543G>A| S292
43966 BAA01g26790-BAA01g26800 A01 15084752 G A intergenic_region MODIFIER n.15084752G>A| S86
43967 BAA01g26790-BAA01g26800 A01 15085552 C T intergenic_region MODIFIER n.15085552C>T| S192
43968 BAA01g26800 A01 15092133 G A downstream_gene_variant MODIFIER c.*3497C>T| S129
43969 BAA01g26800 A01 15094009 G A downstream_gene_variant MODIFIER c.*1621C>T| S280
43970 BAA01g26800 A01 15094261 C T downstream_gene_variant MODIFIER c.*1369G>A| S182
43971 BAA01g26800 A01 15094310 C T downstream_gene_variant MODIFIER c.*1320G>A| S10
43972 BAA01g26800 A01 15094401 G A downstream_gene_variant MODIFIER c.*1229C>T| S202
43973 BAA01g26800 A01 15094535 C T downstream_gene_variant MODIFIER c.*1095G>A| S28
43974 BAA01g26800 A01 15095930 G A missense_variant MODERATE c.883C>T|p.Leu295Phe S180
43975 BAA01g26800 A01 15095974 C T missense_variant MODERATE c.839G>A|p.Arg280Gln S267