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
53251 BAA01g29310 A01 18500416 G A upstream_gene_variant MODIFIER c.-951C>T| S232
53252 BAA01g29310 A01 18500826 G A upstream_gene_variant MODIFIER c.-1361C>T| S246
53253 BAA01g29310 A01 18502443 C T upstream_gene_variant MODIFIER c.-2978G>A| S240
53254 BAA01g29310 A01 18502929 G A upstream_gene_variant MODIFIER c.-3464C>T| S265
53255 BAA01g29310 A01 18503058 T A upstream_gene_variant MODIFIER c.-3593A>T| S257
53256 BAA01g29310-BAA01g29320 A01 18505284 C T intergenic_region MODIFIER n.18505284C>T| S19
53257 BAA01g29310-BAA01g29320 A01 18506080 G A intergenic_region MODIFIER n.18506080G>A| S218
53258 BAA01g29320 A01 18507056 C T upstream_gene_variant MODIFIER c.-4343C>T| S256
53259 BAA01g29320 A01 18507793 A G upstream_gene_variant MODIFIER c.-3606A>G| S166
53260 BAA01g29320 A01 18510684 C T upstream_gene_variant MODIFIER c.-715C>T| S303
53261 BAA01g29320 A01 18510758 G A upstream_gene_variant MODIFIER c.-641G>A| S79
S91
53262 BAA01g29320 A01 18511914 C T synonymous_variant LOW c.516C>T|p.Phe172Phe S107
53263 BAA01g29320 A01 18512284 G A missense_variant MODERATE c.886G>A|p.Glu296Lys S163
53264 BAA01g29320 A01 18512311 G A missense_variant MODERATE c.913G>A|p.Val305Ile S23
53265 BAA01g29320 A01 18513124 C T downstream_gene_variant MODIFIER c.*579C>T| S165
53266 BAA01g29320 A01 18513422 C T downstream_gene_variant MODIFIER c.*877C>T| S275
53267 BAA01g29320 A01 18516190 G A downstream_gene_variant MODIFIER c.*3645G>A| S274
53268 BAA01g29320 A01 18516472 C T downstream_gene_variant MODIFIER c.*3927C>T| S200
53269 BAA01g29320 A01 18516490 C T downstream_gene_variant MODIFIER c.*3945C>T| S142
53270 BAA01g29320 A01 18516570 C T downstream_gene_variant MODIFIER c.*4025C>T| S153
53271 BAA01g29320 A01 18516629 G A downstream_gene_variant MODIFIER c.*4084G>A| S169
53272 BAA01g29320 A01 18516757 G A downstream_gene_variant MODIFIER c.*4212G>A| S259
53273 BAA01g29320 A01 18517465 C T downstream_gene_variant MODIFIER c.*4920C>T| S242
53274 BAA01g29330 A01 18517707 T A downstream_gene_variant MODIFIER c.*3923A>T| S126
53275 BAA01g29330 A01 18518042 G A downstream_gene_variant MODIFIER c.*3588C>T| S65