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
164601 BAA02g10990 A02 4951214 C T upstream_gene_variant MODIFIER c.-4406G>A| S231
S289
S290
164602 BAA02g10990-BAA02g11000 A02 4951867 C T intergenic_region MODIFIER n.4951867C>T| S117
164603 BAA02g11000 A02 4955854 C T upstream_gene_variant MODIFIER c.-4205C>T| S1
S90
164604 BAA02g11000 A02 4956686 C T upstream_gene_variant MODIFIER c.-3373C>T| S185
164605 BAA02g11000 A02 4958230 C T upstream_gene_variant MODIFIER c.-1829C>T| S81
164606 BAA02g11000 A02 4958315 C T upstream_gene_variant MODIFIER c.-1744C>T| S192
164607 BAA02g11000 A02 4958332 C T upstream_gene_variant MODIFIER c.-1727C>T| S44
164608 BAA02g11000 A02 4958366 C T upstream_gene_variant MODIFIER c.-1693C>T| S138
164609 BAA02g11000 A02 4959993 C T upstream_gene_variant MODIFIER c.-66C>T| S195
164610 BAA02g11000 A02 4960078 G A missense_variant MODERATE c.20G>A|p.Ser7Asn S190
164611 BAA02g11010 A02 4964137 G A upstream_gene_variant MODIFIER c.-3606G>A| S274
164612 BAA02g11010 A02 4967272 G A upstream_gene_variant MODIFIER c.-471G>A| S261
164613 BAA02g11020 A02 4968274 G A upstream_gene_variant MODIFIER c.-2746G>A| S168
164614 BAA02g11020 A02 4969331 C T upstream_gene_variant MODIFIER c.-1689C>T| S42
164615 BAA02g11020 A02 4969967 C T upstream_gene_variant MODIFIER c.-1053C>T| S264
164616 BAA02g11020 A02 4971425 G A missense_variant MODERATE c.406G>A|p.Glu136Lys S59
164617 BAA02g11020 A02 4972655 G A missense_variant MODERATE c.781G>A|p.Asp261Asn S155
S211
164618 BAA02g11020 A02 4973089 G A splice_region_variant&intron_variant LOW c.1047+5G>A| S223
164619 BAA02g11020 A02 4973405 G A missense_variant MODERATE c.1159G>A|p.Glu387Lys S295
164620 BAA02g11020 A02 4973740 C T missense_variant MODERATE c.1354C>T|p.Leu452Phe S71
164621 BAA02g11020 A02 4974328 C T downstream_gene_variant MODIFIER c.*3C>T| S58
164622 BAA02g11020 A02 4975844 C T downstream_gene_variant MODIFIER c.*1519C>T| S117
164623 BAA02g11030 A02 4976007 C T synonymous_variant LOW c.582G>A|p.Gln194Gln S76
164624 BAA02g11030 A02 4976225 C T missense_variant MODERATE c.434G>A|p.Arg145Lys S255
164625 BAA02g11030 A02 4976857 G A missense_variant MODERATE c.44C>T|p.Ser15Phe S192