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
116151 BAA10g10140-BAA10g10150 A10 11909953 G A intergenic_region MODIFIER n.11909953G>A| S172
116152 BAA10g10140-BAA10g10150 A10 11909959 G A intergenic_region MODIFIER n.11909959G>A| S174
S216
S265
S27
S39
116153 BAA10g10150 A10 11917144 C T upstream_gene_variant MODIFIER c.-3268C>T| S135
116154 BAA10g10150 A10 11917640 C T upstream_gene_variant MODIFIER c.-2772C>T| S79
S91
116155 BAA10g10150 A10 11917699 G A upstream_gene_variant MODIFIER c.-2713G>A| S278
116156 BAA10g10150 A10 11918240 G A upstream_gene_variant MODIFIER c.-2172G>A| S16
116157 BAA10g10150 A10 11918317 G A upstream_gene_variant MODIFIER c.-2095G>A| S303
116158 BAA10g10150 A10 11918423 C T upstream_gene_variant MODIFIER c.-1989C>T| S114
116159 BAA10g10150 A10 11918837 C T upstream_gene_variant MODIFIER c.-1575C>T| S123
116160 BAA10g10150 A10 11919100 C T upstream_gene_variant MODIFIER c.-1312C>T| S287
116161 BAA10g10150 A10 11920462 C T synonymous_variant LOW c.51C>T|p.Ile17Ile S286
116162 BAA10g10150 A10 11922832 C T synonymous_variant LOW c.1611C>T|p.Val537Val S98
116163 BAA10g10150 A10 11922868 C T synonymous_variant LOW c.1647C>T|p.Phe549Phe S210
S225
116164 BAA10g10150 A10 11922871 C T synonymous_variant LOW c.1650C>T|p.Ser550Ser S19
116165 BAA10g10150 A10 11923734 G A missense_variant MODERATE c.2513G>A|p.Arg838Lys S262
116166 BAA10g10150 A10 11923802 G A missense_variant MODERATE c.2581G>A|p.Gly861Arg S288
116167 BAA10g10150 A10 11926589 C T downstream_gene_variant MODIFIER c.*2491C>T| S38
116168 BAA10g10150 A10 11926605 G A downstream_gene_variant MODIFIER c.*2507G>A| S255
116169 BAA10g10160 A10 11929100 G A downstream_gene_variant MODIFIER c.*4024C>T| S226
116170 BAA10g10160 A10 11929303 C T downstream_gene_variant MODIFIER c.*3821G>A| S287
116171 BAA10g10160 A10 11930202 G A downstream_gene_variant MODIFIER c.*2922C>T| S134
116172 BAA10g10160 A10 11930214 C T downstream_gene_variant MODIFIER c.*2910G>A| S247
116173 BAA10g10160 A10 11930304 C T downstream_gene_variant MODIFIER c.*2820G>A| S183
116174 BAA10g10160 A10 11930387 C T downstream_gene_variant MODIFIER c.*2737G>A| S308
116175 BAA10g10160 A10 11930527 C T downstream_gene_variant MODIFIER c.*2597G>A| S185