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
106151 BAA10g08200 A10 5898642 C T downstream_gene_variant MODIFIER c.*996G>A| S71
106152 BAA10g08200 A10 5899118 G A downstream_gene_variant MODIFIER c.*520C>T| S36
106153 BAA10g08200 A10 5900725 A G synonymous_variant LOW c.1098T>C|p.His366His S26
106154 BAA10g08200 A10 5900742 C T missense_variant MODERATE c.1081G>A|p.Glu361Lys S32
106155 BAA10g08200 A10 5906837 C T upstream_gene_variant MODIFIER c.-4394G>A| S138
S215
S288
106156 BAA10g08200 A10 5906902 G A upstream_gene_variant MODIFIER c.-4459C>T| S118
106157 BAA10g08200 A10 5907420 G A upstream_gene_variant MODIFIER c.-4977C>T| S99
106158 BAA10g08200-BAA10g08210 A10 5907481 G A intergenic_region MODIFIER n.5907481G>A| S157
S163
106159 BAA10g08210 A10 5908255 C T upstream_gene_variant MODIFIER c.-4822C>T| S257
106160 BAA10g08210 A10 5908384 C T upstream_gene_variant MODIFIER c.-4693C>T| S281
106161 BAA10g08210 A10 5908405 C T upstream_gene_variant MODIFIER c.-4672C>T| S269
106162 BAA10g08210 A10 5909251 C T upstream_gene_variant MODIFIER c.-3826C>T| S2
106163 BAA10g08210 A10 5909533 G A upstream_gene_variant MODIFIER c.-3544G>A| S160
106164 BAA10g08210 A10 5910460 G A upstream_gene_variant MODIFIER c.-2617G>A| S86
106165 BAA10g08210 A10 5911400 G A upstream_gene_variant MODIFIER c.-1677G>A| S268
106166 BAA10g08210 A10 5913887 C T synonymous_variant LOW c.285C>T|p.Phe95Phe S117
106167 BAA10g08220 A10 5914536 C T upstream_gene_variant MODIFIER c.-200C>T| S246
106168 BAA10g08220 A10 5914747 G A synonymous_variant LOW c.12G>A|p.Lys4Lys S25
106169 BAA10g08220 A10 5914988 C T missense_variant MODERATE c.253C>T|p.Pro85Ser S155
S211
106170 BAA10g08220 A10 5915051 C T missense_variant MODERATE c.316C>T|p.Leu106Phe S79
S91
106171 BAA10g08220 A10 5915183 C T missense_variant MODERATE c.448C>T|p.Leu150Phe S269
106172 BAA10g08210 A10 5916969 G A downstream_gene_variant MODIFIER c.*3022G>A| S129
106173 BAA10g08210 A10 5917101 G A downstream_gene_variant MODIFIER c.*3154G>A| S33
106174 BAA10g08210 A10 5917294 G A downstream_gene_variant MODIFIER c.*3347G>A| S223
106175 BAA10g08210 A10 5917363 A G downstream_gene_variant MODIFIER c.*3416A>G| S269