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
173001 BAA02g16600 A02 8126308 G A downstream_gene_variant MODIFIER c.*2876G>A| S295
173002 BAA02g16600 A02 8126922 C T downstream_gene_variant MODIFIER c.*3490C>T| S250
173003 BAA02g16600 A02 8126983 C T downstream_gene_variant MODIFIER c.*3551C>T| S182
173004 BAA02g16600 A02 8127614 G A downstream_gene_variant MODIFIER c.*4182G>A| S143
173005 BAA02g16600 A02 8127770 G A downstream_gene_variant MODIFIER c.*4338G>A| S50
173006 BAA02g16610 A02 8130134 C T missense_variant MODERATE c.5938G>A|p.Asp1980Asn S112
173007 BAA02g16610 A02 8132817 G A intron_variant MODIFIER c.5368-2113C>T| S269
173008 BAA02g16610 A02 8133262 G A intron_variant MODIFIER c.5368-2558C>T| S184
173009 BAA02g16610 A02 8134255 C T intron_variant MODIFIER c.5368-3551G>A| S255
173010 BAA02g16610 A02 8134372 C T intron_variant MODIFIER c.5368-3668G>A| S63
173011 BAA02g16610 A02 8134756 C T intron_variant MODIFIER c.5368-4052G>A| S252
173012 BAA02g16610 A02 8135354 G A intron_variant MODIFIER c.5368-4650C>T| S213
173013 BAA02g16610 A02 8135471 G A intron_variant MODIFIER c.5368-4767C>T| S193
173014 BAA02g16610 A02 8135768 C T intron_variant MODIFIER c.5368-5064G>A| S206
S26
173015 BAA02g16610 A02 8136637 C T intron_variant MODIFIER c.5368-5933G>A| S270
173016 BAA02g16610 A02 8138193 C T intron_variant MODIFIER c.5367+6257G>A| S39
173017 BAA02g16610 A02 8138519 C A intron_variant MODIFIER c.5367+5931G>T| S61
173018 BAA02g16610 A02 8138792 G A intron_variant MODIFIER c.5367+5658C>T| S280
173019 BAA02g16610 A02 8139325 C T intron_variant MODIFIER c.5367+5125G>A| S193
173020 BAA02g16610 A02 8139988 C T intron_variant MODIFIER c.5367+4462G>A| S203
173021 BAA02g16610 A02 8140426 C T intron_variant MODIFIER c.5367+4024G>A| S5
173022 BAA02g16610 A02 8140819 G A intron_variant MODIFIER c.5367+3631C>T| S279
173023 BAA02g16610 A02 8141724 G A intron_variant MODIFIER c.5367+2726C>T| S69
173024 BAA02g16610 A02 8143347 G A intron_variant MODIFIER c.5367+1103C>T| S41
173025 BAA02g16610 A02 8144263 A T intron_variant MODIFIER c.5367+187T>A| S274