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 BAA08g05510 A08 4178659 C T upstream_gene_variant MODIFIER c.-3193C>T| S70
2 BAA08g05510 A08 4178912 C T upstream_gene_variant MODIFIER c.-2940C>T| S60
3 BAA08g05510 A08 4179056 C T upstream_gene_variant MODIFIER c.-2796C>T| S120
4 BAA08g05510 A08 4179613 G A upstream_gene_variant MODIFIER c.-2239G>A| S249
5 BAA08g05510 A08 4180161 G A upstream_gene_variant MODIFIER c.-1691G>A| S179
6 BAA08g05510 A08 4180422 G A upstream_gene_variant MODIFIER c.-1430G>A| S33
7 BAA08g05510 A08 4180592 G A upstream_gene_variant MODIFIER c.-1260G>A| S190
8 BAA08g05510 A08 4180938 A G upstream_gene_variant MODIFIER c.-914A>G| S217
9 BAA08g05510 A08 4185878 C T downstream_gene_variant MODIFIER c.*2120C>T| S66
10 BAA08g05510 A08 4185923 G A downstream_gene_variant MODIFIER c.*2165G>A| S263
11 BAA08g05510 A08 4185981 G A downstream_gene_variant MODIFIER c.*2223G>A| S237
12 BAA08g05510 A08 4186496 C T downstream_gene_variant MODIFIER c.*2738C>T| S162
13 BAA08g05510 A08 4188027 G A downstream_gene_variant MODIFIER c.*4269G>A| S269
14 BAA08g05510 A08 4188612 C T downstream_gene_variant MODIFIER c.*4854C>T| S206
S26