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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g29830 A09 20736922 C T upstream_gene_variant MODIFIER c.-4792C>T| S198
2 BAA09g29830 A09 20737097 G A upstream_gene_variant MODIFIER c.-4617G>A| S88
3 BAA09g29830 A09 20737270 C T upstream_gene_variant MODIFIER c.-4444C>T| S302
4 BAA09g29830 A09 20737657 C T upstream_gene_variant MODIFIER c.-4057C>T| S174
S27
5 BAA09g29830 A09 20737798 G A upstream_gene_variant MODIFIER c.-3916G>A| S172
S217
6 BAA09g29830 A09 20738038 G A upstream_gene_variant MODIFIER c.-3676G>A| S98
7 BAA09g29830 A09 20738180 C T upstream_gene_variant MODIFIER c.-3534C>T| S275
8 BAA09g29830 A09 20738499 C T upstream_gene_variant MODIFIER c.-3215C>T| S260
9 BAA09g29830 A09 20738844 C T upstream_gene_variant MODIFIER c.-2870C>T| S136
10 BAA09g29830 A09 20739225 C T upstream_gene_variant MODIFIER c.-2489C>T| S159
S243
S299
11 BAA09g29830 A09 20740833 G T upstream_gene_variant MODIFIER c.-881G>T| S26
12 BAA09g29830 A09 20741820 G A missense_variant MODERATE c.25G>A|p.Val9Ile S236
13 BAA09g29830 A09 20741899 G A missense_variant MODERATE c.104G>A|p.Arg35Lys S298
14 BAA09g29830 A09 20742183 C T downstream_gene_variant MODIFIER c.*109C>T| S276
15 BAA09g29830 A09 20742473 C T downstream_gene_variant MODIFIER c.*399C>T| S12
16 BAA09g29830 A09 20743121 C T downstream_gene_variant MODIFIER c.*1047C>T| S144
17 BAA09g29830 A09 20743142 C T downstream_gene_variant MODIFIER c.*1068C>T| S48
18 BAA09g29830 A09 20743240 C T downstream_gene_variant MODIFIER c.*1166C>T| S159
S243
S299
19 BAA09g29830 A09 20744169 C T downstream_gene_variant MODIFIER c.*2095C>T| S39
20 BAA09g29830 A09 20744682 C T downstream_gene_variant MODIFIER c.*2608C>T| S213
21 BAA09g29830 A09 20744888 G A downstream_gene_variant MODIFIER c.*2814G>A| S210
22 BAA09g29830 A09 20744920 C T downstream_gene_variant MODIFIER c.*2846C>T| S23
23 BAA09g29830 A09 20745630 C T downstream_gene_variant MODIFIER c.*3556C>T| S40