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
173901 BAA02g16980 A02 8422461 G A intron_variant MODIFIER c.277-31C>T| S259
173902 BAA02g16980 A02 8422567 G A missense_variant MODERATE c.220C>T|p.Pro74Ser S290
173903 BAA02g16980 A02 8423022 G A upstream_gene_variant MODIFIER c.-236C>T| S99
173904 BAA02g16980 A02 8424072 G A upstream_gene_variant MODIFIER c.-1286C>T| S294
173905 BAA02g16980 A02 8425292 C T upstream_gene_variant MODIFIER c.-2506G>A| S13
173906 BAA02g16980 A02 8426349 C T upstream_gene_variant MODIFIER c.-3563G>A| S264
173907 BAA02g16990 A02 8428424 C T downstream_gene_variant MODIFIER c.*1335G>A| S152
173908 BAA02g16990 A02 8428628 C T downstream_gene_variant MODIFIER c.*1131G>A| S218
173909 BAA02g16990 A02 8433173 C T upstream_gene_variant MODIFIER c.-3127G>A| S289
S290
173910 BAA02g17000 A02 8435825 G A upstream_gene_variant MODIFIER c.-2485G>A| S67
173911 BAA02g17000 A02 8435926 G A upstream_gene_variant MODIFIER c.-2384G>A| S162
173912 BAA02g17000 A02 8436243 C T upstream_gene_variant MODIFIER c.-2067C>T| S250
173913 BAA02g17000 A02 8437404 G A upstream_gene_variant MODIFIER c.-906G>A| S98
173914 BAA02g17000 A02 8438316 G A missense_variant MODERATE c.7G>A|p.Asp3Asn S286
173915 BAA02g17000 A02 8438482 G A missense_variant MODERATE c.173G>A|p.Gly58Glu S246
173916 BAA02g17000 A02 8438569 G A missense_variant MODERATE c.260G>A|p.Gly87Glu S176
173917 BAA02g17000 A02 8438687 G A missense_variant MODERATE c.286G>A|p.Glu96Lys S168
173918 BAA02g17000 A02 8438793 G A intron_variant MODIFIER c.372+20G>A| S199
173919 BAA02g17000 A02 8439133 C T missense_variant MODERATE c.443C>T|p.Ala148Val S182
173920 BAA02g17000 A02 8439780 G A intron_variant MODIFIER c.875+61G>A| S23
173921 BAA02g17000 A02 8440943 G A synonymous_variant LOW c.1458G>A|p.Leu486Leu S259
173922 BAA02g17000 A02 8441455 C T missense_variant MODERATE c.1885C>T|p.Pro629Ser S100
173923 BAA02g17000 A02 8441456 C T missense_variant MODERATE c.1886C>T|p.Pro629Leu S42
173924 BAA02g17000 A02 8441617 C T missense_variant MODERATE c.2047C>T|p.Pro683Ser S64
173925 BAA02g17000 A02 8442458 G A downstream_gene_variant MODIFIER c.*324G>A| S239