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
170501 BAA02g15100 A02 7223108 G A upstream_gene_variant MODIFIER c.-1726G>A| S169
170502 BAA02g15100 A02 7223967 G A upstream_gene_variant MODIFIER c.-867G>A| S272
170503 BAA02g15100 A02 7223996 C T upstream_gene_variant MODIFIER c.-838C>T| S276
170504 BAA02g15100 A02 7224341 G A upstream_gene_variant MODIFIER c.-493G>A| S38
170505 BAA02g15100 A02 7224687 C T upstream_gene_variant MODIFIER c.-147C>T| S183
S198
170506 BAA02g15100 A02 7224711 G A upstream_gene_variant MODIFIER c.-123G>A| S4
170507 BAA02g15100 A02 7225318 G A missense_variant MODERATE c.485G>A|p.Gly162Glu S155
S211
170508 BAA02g15100 A02 7225712 G A intron_variant MODIFIER c.606+273G>A| S204
170509 BAA02g15100 A02 7226435 C A synonymous_variant LOW c.792C>A|p.Leu264Leu S49
170510 BAA02g15110 A02 7227204 G A upstream_gene_variant MODIFIER c.-3726G>A| S74
170511 BAA02g15100 A02 7228053 G A stop_gained HIGH c.1380G>A|p.Trp460* S261
170512 BAA02g15110 A02 7231199 C T synonymous_variant LOW c.270C>T|p.His90His S171
170513 BAA02g15110 A02 7232303 G A missense_variant MODERATE c.691G>A|p.Asp231Asn S89
170514 BAA02g15110 A02 7232449 G A synonymous_variant LOW c.837G>A|p.Glu279Glu S193
170515 BAA02g15110 A02 7235096 G A downstream_gene_variant MODIFIER c.*2641G>A| S173
170516 BAA02g15110 A02 7235766 C T downstream_gene_variant MODIFIER c.*3311C>T| S32
170517 BAA02g15110 A02 7236364 C T downstream_gene_variant MODIFIER c.*3909C>T| S179
170518 BAA02g15110 A02 7236712 G A downstream_gene_variant MODIFIER c.*4257G>A| S208
S93
170519 BAA02g15110 A02 7236925 C T downstream_gene_variant MODIFIER c.*4470C>T| S181
170520 BAA02g15120 A02 7237584 G A downstream_gene_variant MODIFIER c.*1200C>T| S41
170521 BAA02g15120 A02 7239189 G A intron_variant MODIFIER c.777+28C>T| S297
170522 BAA02g15120 A02 7239522 G A synonymous_variant LOW c.564C>T|p.Thr188Thr S187
170523 BAA02g15120 A02 7239942 G A intron_variant MODIFIER c.399-255C>T| S12
170524 BAA02g15120 A02 7240436 G A missense_variant MODERATE c.211C>T|p.Pro71Ser S122
170525 BAA02g15120 A02 7240564 G A missense_variant MODERATE c.83C>T|p.Ala28Val S187