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
41401 BAA01g25940 A01 14299943 C T upstream_gene_variant MODIFIER c.-1140G>A| S256
41402 BAA01g25940 A01 14300537 C T upstream_gene_variant MODIFIER c.-1734G>A| S282
41403 BAA01g25940 A01 14301842 C T upstream_gene_variant MODIFIER c.-3039G>A| S267
41404 BAA01g25940 A01 14301889 G A upstream_gene_variant MODIFIER c.-3086C>T| S197
41405 BAA01g25940 A01 14302202 G A upstream_gene_variant MODIFIER c.-3399C>T| S209
41406 BAA01g25940 A01 14302874 C T upstream_gene_variant MODIFIER c.-4071G>A| S198
41407 BAA01g25940 A01 14303032 C T upstream_gene_variant MODIFIER c.-4229G>A| S158
41408 BAA01g25950 A01 14304058 C T upstream_gene_variant MODIFIER c.-2127C>T| S112
41409 BAA01g25950 A01 14304847 G A upstream_gene_variant MODIFIER c.-1338G>A| S262
41410 BAA01g25950 A01 14305287 A G upstream_gene_variant MODIFIER c.-898A>G| S48
41411 BAA01g25950 A01 14306362 G A missense_variant MODERATE c.178G>A|p.Val60Met S275
41412 BAA01g25950 A01 14306376 C T synonymous_variant LOW c.192C>T|p.Tyr64Tyr S237
41413 BAA01g25960 A01 14307036 G A downstream_gene_variant MODIFIER c.*4927C>T| S17
41414 BAA01g25960 A01 14307380 C T downstream_gene_variant MODIFIER c.*4583G>A| S221
41415 BAA01g25950 A01 14309293 C T synonymous_variant LOW c.1503C>T|p.Phe501Phe S230
41416 BAA01g25950 A01 14309541 C T missense_variant MODERATE c.1751C>T|p.Ser584Leu S192
41417 BAA01g25960 A01 14309771 G A downstream_gene_variant MODIFIER c.*2192C>T| S156
41418 BAA01g25960 A01 14309879 G A downstream_gene_variant MODIFIER c.*2084C>T| S144
41419 BAA01g25950 A01 14310818 C T missense_variant MODERATE c.2624C>T|p.Ser875Leu S166
41420 BAA01g25950 A01 14311048 G A downstream_gene_variant MODIFIER c.*43G>A| S139
41421 BAA01g25950 A01 14311286 C T downstream_gene_variant MODIFIER c.*281C>T| S210
41422 BAA01g25950 A01 14311410 C T downstream_gene_variant MODIFIER c.*405C>T| S261
41423 BAA01g25960 A01 14311992 C T missense_variant MODERATE c.352G>A|p.Ala118Thr S279
41424 BAA01g25960 A01 14312085 C T missense_variant MODERATE c.259G>A|p.Val87Ile S208
S93
41425 BAA01g25950 A01 14312168 G A downstream_gene_variant MODIFIER c.*1163G>A| S202