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
198201 BAA02g29660 A02 17003871 C T upstream_gene_variant MODIFIER c.-444G>A| S286
198202 BAA02g29660 A02 17004665 C T upstream_gene_variant MODIFIER c.-1238G>A| S289
S290
198203 BAA02g29660 A02 17005327 G A upstream_gene_variant MODIFIER c.-1900C>T| S298
198204 BAA02g29660 A02 17005580 G A upstream_gene_variant MODIFIER c.-2153C>T| S36
198205 BAA02g29660 A02 17005714 G A upstream_gene_variant MODIFIER c.-2287C>T| S155
S211
198206 BAA02g29660 A02 17005756 C T upstream_gene_variant MODIFIER c.-2329G>A| S283
198207 BAA02g29660 A02 17005854 G A upstream_gene_variant MODIFIER c.-2427C>T| S70
198208 BAA02g29660 A02 17006835 C T upstream_gene_variant MODIFIER c.-3408G>A| S270
198209 BAA02g29660 A02 17007032 G A upstream_gene_variant MODIFIER c.-3605C>T| S43
198210 BAA02g29660 A02 17008071 G A upstream_gene_variant MODIFIER c.-4644C>T| S129
198211 BAA02g29660 A02 17008164 G A upstream_gene_variant MODIFIER c.-4737C>T| S48
198212 BAA02g29670 A02 17008807 C T downstream_gene_variant MODIFIER c.*2165G>A| S2
198213 BAA02g29670 A02 17010354 C T downstream_gene_variant MODIFIER c.*618G>A| S138
198214 BAA02g29670 A02 17010516 C T downstream_gene_variant MODIFIER c.*456G>A| S15
198215 BAA02g29670 A02 17010567 C T downstream_gene_variant MODIFIER c.*405G>A| S92
198216 BAA02g29670 A02 17011148 G A intron_variant MODIFIER c.2560-93C>T| S41
198217 BAA02g29670 A02 17011726 C T missense_variant MODERATE c.2299G>A|p.Glu767Lys S177
198218 BAA02g29670 A02 17012247 G A intron_variant MODIFIER c.2007+20C>T| S205
198219 BAA02g29670 A02 17012753 G A synonymous_variant LOW c.1671C>T|p.Leu557Leu S133
198220 BAA02g29670 A02 17013614 C T missense_variant MODERATE c.1117G>A|p.Ala373Thr S142
198221 BAA02g29670 A02 17013915 C T stop_gained HIGH c.900G>A|p.Trp300* S266
198222 BAA02g29670 A02 17014430 C T intron_variant MODIFIER c.691-20G>A| S54
198223 BAA02g29670 A02 17014442 G A intron_variant MODIFIER c.691-32C>T| S38
198224 BAA02g29670 A02 17015002 G A missense_variant MODERATE c.509C>T|p.Thr170Ile S245
198225 BAA02g29670 A02 17015330 C T splice_donor_variant&intron_variant HIGH c.345+1G>A| S185