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
52151 BAA01g28770 A01 18075773 G A missense_variant MODERATE c.1961G>A|p.Arg654His S294
52152 BAA01g28770 A01 18075883 G A missense_variant MODERATE c.2071G>A|p.Ala691Thr S281
52153 BAA01g28780 A01 18077371 C T downstream_gene_variant MODIFIER c.*3318G>A| S250
52154 BAA01g28780 A01 18077441 G A downstream_gene_variant MODIFIER c.*3248C>T| S263
52155 BAA01g28780 A01 18078457 G A downstream_gene_variant MODIFIER c.*2232C>T| S144
52156 BAA01g28780 A01 18078546 C T downstream_gene_variant MODIFIER c.*2143G>A| S161
52157 BAA01g28780 A01 18078709 G A downstream_gene_variant MODIFIER c.*1980C>T| S36
52158 BAA01g28780 A01 18078807 G A downstream_gene_variant MODIFIER c.*1882C>T| S191
52159 BAA01g28770 A01 18080302 G A downstream_gene_variant MODIFIER c.*224G>A| S197
52160 BAA01g28780 A01 18080721 C T missense_variant MODERATE c.1042G>A|p.Glu348Lys S167
52161 BAA01g28780 A01 18080772 C T missense_variant MODERATE c.991G>A|p.Asp331Asn S230
52162 BAA01g28780 A01 18080882 G A missense_variant MODERATE c.881C>T|p.Pro294Leu S19
52163 BAA01g28780 A01 18081241 C T synonymous_variant LOW c.522G>A|p.Lys174Lys S240
52164 BAA01g28780 A01 18081246 C T missense_variant MODERATE c.517G>A|p.Val173Ile S198
52165 BAA01g28780 A01 18081744 C T missense_variant MODERATE c.19G>A|p.Val7Ile S284
52166 BAA01g28780 A01 18081804 G A upstream_gene_variant MODIFIER c.-42C>T| S236
52167 BAA01g28780 A01 18082077 C T upstream_gene_variant MODIFIER c.-315G>A| S286
52168 BAA01g28780 A01 18082153 C T upstream_gene_variant MODIFIER c.-391G>A| S241
S27
S39
52169 BAA01g28780 A01 18082156 C T upstream_gene_variant MODIFIER c.-394G>A| S164
52170 BAA01g28780 A01 18082184 C T upstream_gene_variant MODIFIER c.-422G>A| S42
52171 BAA01g28780 A01 18082197 G A upstream_gene_variant MODIFIER c.-435C>T| S288
52172 BAA01g28780 A01 18082230 C T upstream_gene_variant MODIFIER c.-468G>A| S286
52173 BAA01g28780 A01 18082843 G A upstream_gene_variant MODIFIER c.-1081C>T| S298
52174 BAA01g28780 A01 18085023 C T upstream_gene_variant MODIFIER c.-3261G>A| S125
52175 BAA01g28790 A01 18086907 C T upstream_gene_variant MODIFIER c.-1868C>T| S118