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
194251 BAA02g27820-BAA02g27830 A02 15671179 G A intergenic_region MODIFIER n.15671179G>A| S240
194252 BAA02g27820-BAA02g27830 A02 15671214 G A intergenic_region MODIFIER n.15671214G>A| S238
194253 BAA02g27830 A02 15681231 C T downstream_gene_variant MODIFIER c.*2276G>A| S270
194254 BAA02g27830 A02 15681424 C T downstream_gene_variant MODIFIER c.*2083G>A| S54
194255 BAA02g27830 A02 15681486 G A downstream_gene_variant MODIFIER c.*2021C>T| S272
194256 BAA02g27830 A02 15681512 G A downstream_gene_variant MODIFIER c.*1995C>T| S149
194257 BAA02g27830 A02 15681637 C T downstream_gene_variant MODIFIER c.*1870G>A| S265
S39
194258 BAA02g27830 A02 15681752 C T downstream_gene_variant MODIFIER c.*1755G>A| S268
194259 BAA02g27830 A02 15681753 C T downstream_gene_variant MODIFIER c.*1754G>A| S181
194260 BAA02g27830 A02 15682175 G A downstream_gene_variant MODIFIER c.*1332C>T| S217
S248
194261 BAA02g27830 A02 15683640 C T missense_variant MODERATE c.1271G>A|p.Gly424Glu S46
194262 BAA02g27830 A02 15684079 C T missense_variant MODERATE c.832G>A|p.Asp278Asn S63
194263 BAA02g27830 A02 15684094 C T missense_variant MODERATE c.817G>A|p.Gly273Ser S77
S82
194264 BAA02g27830 A02 15684321 G A missense_variant MODERATE c.590C>T|p.Thr197Ile S38
194265 BAA02g27830 A02 15684521 G A synonymous_variant LOW c.390C>T|p.Asn130Asn S160
194266 BAA02g27840 A02 15686106 C T missense_variant MODERATE c.1267G>A|p.Glu423Lys S207
194267 BAA02g27840 A02 15687312 C T missense_variant MODERATE c.574G>A|p.Asp192Asn S139
194268 BAA02g27830 A02 15687363 G A upstream_gene_variant MODIFIER c.-2453C>T| S86
194269 BAA02g27840 A02 15687757 G A missense_variant MODERATE c.389C>T|p.Ser130Phe S81
S85
194270 BAA02g27840 A02 15687774 C T synonymous_variant LOW c.372G>A|p.Arg124Arg S171
194271 BAA02g27830 A02 15688841 G A upstream_gene_variant MODIFIER c.-3931C>T| S139
194272 BAA02g27850 A02 15689099 G A splice_region_variant&intron_variant LOW c.993+7C>T| S292
194273 BAA02g27850 A02 15689899 C T missense_variant MODERATE c.560G>A|p.Arg187Lys S88
194274 BAA02g27850 A02 15690472 G A synonymous_variant LOW c.237C>T|p.Phe79Phe S295
194275 BAA02g27840 A02 15691829 C T upstream_gene_variant MODIFIER c.-3504G>A| S15