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
11201 BAA01g09110 A01 3993559 C T upstream_gene_variant MODIFIER c.-1949G>A| S54
11202 BAA01g09110 A01 3993779 A G upstream_gene_variant MODIFIER c.-2169T>C| S4
11203 BAA01g09110 A01 3994176 C T upstream_gene_variant MODIFIER c.-2566G>A| S140
11204 BAA01g09110 A01 3994417 C T upstream_gene_variant MODIFIER c.-2807G>A| S50
11205 BAA01g09110 A01 3994843 C T upstream_gene_variant MODIFIER c.-3233G>A| S117
11206 BAA01g09110 A01 3995397 A C upstream_gene_variant MODIFIER c.-3787T>G| S233
11207 BAA01g09110 A01 3996145 C T upstream_gene_variant MODIFIER c.-4535G>A| S303
11208 BAA01g09120 A01 3996484 C T synonymous_variant LOW c.33G>A|p.Leu11Leu S263
11209 BAA01g09120 A01 3996873 C T upstream_gene_variant MODIFIER c.-357G>A| S61
11210 BAA01g09120 A01 3997475 C T upstream_gene_variant MODIFIER c.-959G>A| S134
11211 BAA01g09130 A01 3997567 C T missense_variant MODERATE c.706G>A|p.Gly236Arg S50
11212 BAA01g09120 A01 3999075 C T upstream_gene_variant MODIFIER c.-2559G>A| S65
11213 BAA01g09120 A01 4001211 C T upstream_gene_variant MODIFIER c.-4695G>A| S62
11214 BAA01g09130 A01 4002602 G T upstream_gene_variant MODIFIER c.-3158C>A| S223
11215 BAA01g09130 A01 4003189 C T upstream_gene_variant MODIFIER c.-3745G>A| S38
11216 BAA01g09130 A01 4003226 C T upstream_gene_variant MODIFIER c.-3782G>A| S304
11217 BAA01g09130 A01 4003335 C T upstream_gene_variant MODIFIER c.-3891G>A| S120
11218 BAA01g09130 A01 4003610 G A upstream_gene_variant MODIFIER c.-4166C>T| S297
11219 BAA01g09130 A01 4003694 G A upstream_gene_variant MODIFIER c.-4250C>T| S173
11220 BAA01g09130 A01 4003887 G A upstream_gene_variant MODIFIER c.-4443C>T| S190
11221 BAA01g09140 A01 4004863 G A upstream_gene_variant MODIFIER c.-1050G>A| S203
11222 BAA01g09140 A01 4006432 C T missense_variant MODERATE c.520C>T|p.Pro174Ser S244
11223 BAA01g09140 A01 4006538 C T intron_variant MODIFIER c.602+24C>T| S198
11224 BAA01g09140 A01 4008158 C T missense_variant MODERATE c.1058C>T|p.Pro353Leu S152
11225 BAA01g09140 A01 4008354 C T synonymous_variant LOW c.1254C>T|p.Asp418Asp S250