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


Gene ID

Results: 1 - 21 of 21 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA03g66730 A03 41148250 G A upstream_gene_variant MODIFIER c.-2569G>A| S146
2 BAA03g66730 A03 41148476 G A upstream_gene_variant MODIFIER c.-2343G>A| S127
S45
3 BAA03g66730 A03 41148694 C T upstream_gene_variant MODIFIER c.-2125C>T| S59
4 BAA03g66730 A03 41149206 C T upstream_gene_variant MODIFIER c.-1613C>T| S111
5 BAA03g66730 A03 41149452 G A upstream_gene_variant MODIFIER c.-1367G>A| S268
6 BAA03g66730 A03 41150089 C T upstream_gene_variant MODIFIER c.-730C>T| S47
7 BAA03g66730 A03 41150313 C T upstream_gene_variant MODIFIER c.-506C>T| S61
8 BAA03g66730 A03 41150406 G A upstream_gene_variant MODIFIER c.-413G>A| S150
9 BAA03g66730 A03 41150408 C T upstream_gene_variant MODIFIER c.-411C>T| S10
10 BAA03g66730 A03 41150705 G A upstream_gene_variant MODIFIER c.-114G>A| S206
S26
11 BAA03g66730 A03 41151328 G A missense_variant MODERATE c.262G>A|p.Ala88Thr S152
12 BAA03g66730 A03 41152804 C T downstream_gene_variant MODIFIER c.*446C>T| S199
13 BAA03g66730 A03 41152806 G A downstream_gene_variant MODIFIER c.*448G>A| S278
14 BAA03g66730 A03 41153110 C T downstream_gene_variant MODIFIER c.*752C>T| S19
15 BAA03g66730 A03 41154175 T C downstream_gene_variant MODIFIER c.*1817T>C| S297
16 BAA03g66730 A03 41154429 G A downstream_gene_variant MODIFIER c.*2071G>A| S242
17 BAA03g66730 A03 41154743 C T downstream_gene_variant MODIFIER c.*2385C>T| S149
18 BAA03g66730 A03 41155454 C T downstream_gene_variant MODIFIER c.*3096C>T| S306
S308
19 BAA03g66730 A03 41156757 G A downstream_gene_variant MODIFIER c.*4399G>A| S96
20 BAA03g66730 A03 41157040 C T downstream_gene_variant MODIFIER c.*4682C>T| S8
21 BAA03g66730 A03 41157217 C T downstream_gene_variant MODIFIER c.*4859C>T| S192