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 BAA08g11580 A08 10240048 G A downstream_gene_variant MODIFIER c.*4661C>T| S306
S308
2 BAA08g11580 A08 10240722 C T downstream_gene_variant MODIFIER c.*3987G>A| S50
3 BAA08g11580 A08 10241073 G A downstream_gene_variant MODIFIER c.*3636C>T| S165
4 BAA08g11580 A08 10241341 G A downstream_gene_variant MODIFIER c.*3368C>T| S12
5 BAA08g11580 A08 10242159 C T downstream_gene_variant MODIFIER c.*2550G>A| S60
6 BAA08g11580 A08 10243759 G A downstream_gene_variant MODIFIER c.*950C>T| S37
7 BAA08g11580 A08 10245474 C T synonymous_variant LOW c.60G>A|p.Arg20Arg S144
8 BAA08g11580 A08 10246601 C T upstream_gene_variant MODIFIER c.-876G>A| S140
9 BAA08g11580 A08 10246921 C T upstream_gene_variant MODIFIER c.-1196G>A| S140
10 BAA08g11580 A08 10247944 C T upstream_gene_variant MODIFIER c.-2219G>A| S201
11 BAA08g11580 A08 10249792 C T upstream_gene_variant MODIFIER c.-4067G>A| S302
12 BAA08g11580 A08 10250012 G A upstream_gene_variant MODIFIER c.-4287C>T| S287
13 BAA08g11580 A08 10250096 C T upstream_gene_variant MODIFIER c.-4371G>A| S262
14 BAA08g11580 A08 10250388 G A upstream_gene_variant MODIFIER c.-4663C>T| S286