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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAS13g00660 Scaffold13 7781216 C T upstream_gene_variant MODIFIER c.-4289C>T| S61
2 BAS13g00660 Scaffold13 7781626 G A upstream_gene_variant MODIFIER c.-3879G>A| S151
S263
3 BAS13g00660 Scaffold13 7781911 C T upstream_gene_variant MODIFIER c.-3594C>T| S191
4 BAS13g00660 Scaffold13 7782044 C T upstream_gene_variant MODIFIER c.-3461C>T| S182
5 BAS13g00660 Scaffold13 7782655 A C upstream_gene_variant MODIFIER c.-2850A>C| S242
S256
6 BAS13g00660 Scaffold13 7783306 C T upstream_gene_variant MODIFIER c.-2199C>T| S125
7 BAS13g00660 Scaffold13 7784140 G A upstream_gene_variant MODIFIER c.-1365G>A| S167
8 BAS13g00660 Scaffold13 7784175 T G upstream_gene_variant MODIFIER c.-1330T>G| S167
9 BAS13g00660 Scaffold13 7784227 C T upstream_gene_variant MODIFIER c.-1278C>T| S51
10 BAS13g00660 Scaffold13 7784432 G A upstream_gene_variant MODIFIER c.-1073G>A| S113
11 BAS13g00660 Scaffold13 7784916 G A upstream_gene_variant MODIFIER c.-589G>A| S187
12 BAS13g00660 Scaffold13 7785370 C T upstream_gene_variant MODIFIER c.-135C>T| S133
13 BAS13g00660 Scaffold13 7786045 G A missense_variant MODERATE c.226G>A|p.Ala76Thr S15
S3
14 BAS13g00660 Scaffold13 7788731 C T downstream_gene_variant MODIFIER c.*483C>T| S72
S78
15 BAS13g00660 Scaffold13 7789230 G A downstream_gene_variant MODIFIER c.*982G>A| S156
16 BAS13g00660 Scaffold13 7789675 C T downstream_gene_variant MODIFIER c.*1427C>T| S133