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
171051 BAA02g15440 A02 7440483 G A intron_variant MODIFIER c.1241+12C>T| S87
171052 BAA02g15440 A02 7441085 C T intron_variant MODIFIER c.926-36G>A| S167
171053 BAA02g15440 A02 7442202 G A synonymous_variant LOW c.393C>T|p.Ile131Ile S238
171054 BAA02g15440 A02 7442302 C T missense_variant MODERATE c.293G>A|p.Arg98Lys S273
171055 BAA02g15440 A02 7444439 C T upstream_gene_variant MODIFIER c.-1683G>A| S301
S304
171056 BAA02g15440 A02 7444873 C T upstream_gene_variant MODIFIER c.-2117G>A| S199
171057 BAA02g15440 A02 7445154 C T upstream_gene_variant MODIFIER c.-2398G>A| S123
171058 BAA02g15440 A02 7445200 C T upstream_gene_variant MODIFIER c.-2444G>A| S270
171059 BAA02g15440 A02 7446015 G A upstream_gene_variant MODIFIER c.-3259C>T| S105
171060 BAA02g15440 A02 7446129 C T upstream_gene_variant MODIFIER c.-3373G>A| S183
S198
171061 BAA02g15450 A02 7447190 C T synonymous_variant LOW c.1059G>A|p.Arg353Arg S183
S198
171062 BAA02g15450 A02 7448409 G A upstream_gene_variant MODIFIER c.-50C>T| S291
171063 BAA02g15450 A02 7450188 T C upstream_gene_variant MODIFIER c.-1829A>G| S282
171064 BAA02g15450 A02 7450457 G A upstream_gene_variant MODIFIER c.-2098C>T| S153
S213
171065 BAA02g15450 A02 7450788 G A upstream_gene_variant MODIFIER c.-2429C>T| S122
171066 BAA02g15450 A02 7452590 G A upstream_gene_variant MODIFIER c.-4231C>T| S289
S290
171067 BAA02g15450-BAA02g15460 A02 7453531 G A intergenic_region MODIFIER n.7453531G>A| S140
171068 BAA02g15460 A02 7458598 C T downstream_gene_variant MODIFIER c.*2547G>A| S49
171069 BAA02g15460 A02 7458915 G A downstream_gene_variant MODIFIER c.*2230C>T| S206
171070 BAA02g15460 A02 7459140 C T downstream_gene_variant MODIFIER c.*2005G>A| S87
171071 BAA02g15460 A02 7459574 G A downstream_gene_variant MODIFIER c.*1571C>T| S190
171072 BAA02g15460 A02 7459779 C T downstream_gene_variant MODIFIER c.*1366G>A| S66
171073 BAA02g15460 A02 7459806 G A downstream_gene_variant MODIFIER c.*1339C>T| S11
171074 BAA02g15460 A02 7460302 C T downstream_gene_variant MODIFIER c.*843G>A| S234
171075 BAA02g15460 A02 7460967 C T downstream_gene_variant MODIFIER c.*178G>A| S46