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
179251 BAA02g19750 A02 10319428 C T downstream_gene_variant MODIFIER c.*1396C>T| S40
S49
179252 BAA02g19750 A02 10319922 C T downstream_gene_variant MODIFIER c.*1890C>T| S15
S3
179253 BAA02g19750 A02 10320277 G A downstream_gene_variant MODIFIER c.*2245G>A| S53
179254 BAA02g19750 A02 10320412 G A downstream_gene_variant MODIFIER c.*2380G>A| S287
179255 BAA02g19750 A02 10320508 G A downstream_gene_variant MODIFIER c.*2476G>A| S247
179256 BAA02g19750 A02 10320802 C T downstream_gene_variant MODIFIER c.*2770C>T| S290
179257 BAA02g19750 A02 10320880 C T downstream_gene_variant MODIFIER c.*2848C>T| S286
179258 BAA02g19750 A02 10321861 C T downstream_gene_variant MODIFIER c.*3829C>T| S276
179259 BAA02g19760 A02 10323893 G A missense_variant MODERATE c.316C>T|p.Pro106Ser S166
179260 BAA02g19760 A02 10324066 C T synonymous_variant LOW c.255G>A|p.Arg85Arg S32
179261 BAA02g19760 A02 10324236 C T intron_variant MODIFIER c.205+83G>A| S103
179262 BAA02g19760 A02 10326944 C T upstream_gene_variant MODIFIER c.-2421G>A| S281
179263 BAA02g19760 A02 10326962 G A upstream_gene_variant MODIFIER c.-2439C>T| S287
179264 BAA02g19760 A02 10327626 C G upstream_gene_variant MODIFIER c.-3103G>C| S6
179265 BAA02g19760 A02 10328497 C T upstream_gene_variant MODIFIER c.-3974G>A| S268
179266 BAA02g19770 A02 10331162 C T upstream_gene_variant MODIFIER c.-1669C>T| S261
179267 BAA02g19770 A02 10331372 C T upstream_gene_variant MODIFIER c.-1459C>T| S221
179268 BAA02g19770 A02 10332906 G A missense_variant MODERATE c.76G>A|p.Glu26Lys S50
179269 BAA02g19770 A02 10334564 G A downstream_gene_variant MODIFIER c.*1491G>A| S150
179270 BAA02g19770 A02 10334659 G A downstream_gene_variant MODIFIER c.*1586G>A| S150
179271 BAA02g19770 A02 10336078 G A downstream_gene_variant MODIFIER c.*3005G>A| S69
179272 BAA02g19780 A02 10338691 C T downstream_gene_variant MODIFIER c.*1125G>A| S212
179273 BAA02g19780 A02 10339032 G A downstream_gene_variant MODIFIER c.*784C>T| S278
179274 BAA02g19780 A02 10339305 G A downstream_gene_variant MODIFIER c.*511C>T| S280
179275 BAA02g19780 A02 10340009 G A missense_variant MODERATE c.170C>T|p.Ser57Phe S259