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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g44950 A02 36913603 C T upstream_gene_variant MODIFIER c.-4469C>T| S142
2 BAA02g44950 A02 36913646 C T upstream_gene_variant MODIFIER c.-4426C>T| S183
S198
3 BAA02g44950 A02 36915477 C T upstream_gene_variant MODIFIER c.-2595C>T| S68
4 BAA02g44950 A02 36916487 C T upstream_gene_variant MODIFIER c.-1585C>T| S47
5 BAA02g44950 A02 36916626 C T upstream_gene_variant MODIFIER c.-1446C>T| S48
6 BAA02g44950 A02 36917282 G A upstream_gene_variant MODIFIER c.-790G>A| S132
S137
S215
7 BAA02g44950 A02 36917661 G A upstream_gene_variant MODIFIER c.-411G>A| S251
8 BAA02g44950 A02 36917790 C T upstream_gene_variant MODIFIER c.-282C>T| S184
9 BAA02g44950 A02 36918078 G A missense_variant MODERATE c.7G>A|p.Asp3Asn S60
10 BAA02g44950 A02 36919464 C T downstream_gene_variant MODIFIER c.*532C>T| S33
11 BAA02g44950 A02 36919684 C T downstream_gene_variant MODIFIER c.*752C>T| S142
12 BAA02g44950 A02 36920659 G A downstream_gene_variant MODIFIER c.*1727G>A| S199
13 BAA02g44950 A02 36920661 G A downstream_gene_variant MODIFIER c.*1729G>A| S217
14 BAA02g44950 A02 36920786 C T downstream_gene_variant MODIFIER c.*1854C>T| S104
S52
15 BAA02g44950 A02 36920907 G A downstream_gene_variant MODIFIER c.*1975G>A| S62
16 BAA02g44950 A02 36922443 C T downstream_gene_variant MODIFIER c.*3511C>T| S61
17 BAA02g44950 A02 36922995 C T downstream_gene_variant MODIFIER c.*4063C>T| S221
18 BAA02g44950 A02 36923576 C T downstream_gene_variant MODIFIER c.*4644C>T| S270
19 BAA02g44950 A02 36923654 C T downstream_gene_variant MODIFIER c.*4722C>T| S100