Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g39350 A02 33437371 G A upstream_gene_variant MODIFIER c.-1622G>A| S251
2 BAA02g39350 A02 33437444 C T upstream_gene_variant MODIFIER c.-1549C>T| S296
3 BAA02g39350 A02 33438168 C T upstream_gene_variant MODIFIER c.-825C>T| S195
4 BAA02g39350 A02 33438996 G A missense_variant MODERATE c.4G>A|p.Gly2Arg S266
5 BAA02g39350 A02 33440293 C T downstream_gene_variant MODIFIER c.*953C>T| S140
S78
6 BAA02g39350 A02 33441132 G A downstream_gene_variant MODIFIER c.*1792G>A| S187
7 BAA02g39350 A02 33441303 C T downstream_gene_variant MODIFIER c.*1963C>T| S116
8 BAA02g39350 A02 33441396 G A downstream_gene_variant MODIFIER c.*2056G>A| S142
9 BAA02g39350 A02 33441784 C T downstream_gene_variant MODIFIER c.*2444C>T| S61
10 BAA02g39350 A02 33441855 G A downstream_gene_variant MODIFIER c.*2515G>A| S80
11 BAA02g39350 A02 33442204 G A downstream_gene_variant MODIFIER c.*2864G>A| S17
12 BAA02g39350 A02 33442743 G A downstream_gene_variant MODIFIER c.*3403G>A| S276
13 BAA02g39350 A02 33442977 C T downstream_gene_variant MODIFIER c.*3637C>T| S260
14 BAA02g39350 A02 33443813 C T downstream_gene_variant MODIFIER c.*4473C>T| S226