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
190951 BAA02g26150 A02 14493195 C T upstream_gene_variant MODIFIER c.-1010G>A| S41
190952 BAA02g26150 A02 14494289 G A upstream_gene_variant MODIFIER c.-2104C>T| S109
190953 BAA02g26150 A02 14494756 C T upstream_gene_variant MODIFIER c.-2571G>A| S171
190954 BAA02g26150 A02 14495324 G A upstream_gene_variant MODIFIER c.-3139C>T| S25
190955 BAA02g26150 A02 14495456 G A upstream_gene_variant MODIFIER c.-3271C>T| S169
190956 BAA02g26150 A02 14496531 G A upstream_gene_variant MODIFIER c.-4346C>T| S203
190957 BAA02g26160 A02 14497984 C T downstream_gene_variant MODIFIER c.*2087G>A| S138
190958 BAA02g26160 A02 14498093 G A downstream_gene_variant MODIFIER c.*1978C>T| S57
190959 BAA02g26160 A02 14498208 G A downstream_gene_variant MODIFIER c.*1863C>T| S200
190960 BAA02g26160 A02 14498219 G A downstream_gene_variant MODIFIER c.*1852C>T| S236
190961 BAA02g26160 A02 14499271 C T downstream_gene_variant MODIFIER c.*800G>A| S240
190962 BAA02g26160 A02 14499362 C T downstream_gene_variant MODIFIER c.*709G>A| S250
190963 BAA02g26160 A02 14500050 G A downstream_gene_variant MODIFIER c.*21C>T| S159
S243
190964 BAA02g26160 A02 14500802 C T upstream_gene_variant MODIFIER c.-204G>A| S66
190965 BAA02g26160 A02 14501330 G A upstream_gene_variant MODIFIER c.-732C>T| S111
190966 BAA02g26160 A02 14501342 C T upstream_gene_variant MODIFIER c.-744G>A| S176
S221
190967 BAA02g26160 A02 14501701 G A upstream_gene_variant MODIFIER c.-1103C>T| S288
190968 BAA02g26160 A02 14501795 G A upstream_gene_variant MODIFIER c.-1197C>T| S119
190969 BAA02g26160 A02 14501936 C T upstream_gene_variant MODIFIER c.-1338G>A| S233
190970 BAA02g26160 A02 14501948 C T upstream_gene_variant MODIFIER c.-1350G>A| S174
S216
S27
190971 BAA02g26250 A02 14554864 G A missense_variant MODERATE c.827G>A|p.Gly276Glu S259
190972 BAA02g26250 A02 14555625 C T synonymous_variant LOW c.1122C>T|p.Ser374Ser S122
190973 BAA02g26250 A02 14555757 G A downstream_gene_variant MODIFIER c.*21G>A| S155
S211
190974 BAA02g26250 A02 14555908 G A downstream_gene_variant MODIFIER c.*172G>A| S103
190975 BAA02g26250 A02 14556198 C T downstream_gene_variant MODIFIER c.*462C>T| S286