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 BAA09g31790 A09 40091069 G A upstream_gene_variant MODIFIER c.-4504G>A| S162
2 BAA09g31790 A09 40091294 C T upstream_gene_variant MODIFIER c.-4279C>T| S19
3 BAA09g31790 A09 40091309 G A upstream_gene_variant MODIFIER c.-4264G>A| S33
4 BAA09g31790 A09 40091374 C T upstream_gene_variant MODIFIER c.-4199C>T| S146
5 BAA09g31790 A09 40091551 G A upstream_gene_variant MODIFIER c.-4022G>A| S288
6 BAA09g31790 A09 40091854 G A upstream_gene_variant MODIFIER c.-3719G>A| S41
7 BAA09g31790 A09 40093955 G A upstream_gene_variant MODIFIER c.-1618G>A| S48
8 BAA09g31790 A09 40094286 C T upstream_gene_variant MODIFIER c.-1287C>T| S182
9 BAA09g31790 A09 40094301 C T upstream_gene_variant MODIFIER c.-1272C>T| S236
10 BAA09g31790 A09 40097240 G A synonymous_variant LOW c.219G>A|p.Leu73Leu S112
11 BAA09g31790 A09 40098126 G A missense_variant MODERATE c.1105G>A|p.Val369Ile S161
12 BAA09g31790 A09 40098257 G T missense_variant MODERATE c.1236G>T|p.Lys412Asn S6
13 BAA09g31790 A09 40098998 G A stop_gained HIGH c.1353G>A|p.Trp451* S33
14 BAA09g31790 A09 40101793 C T downstream_gene_variant MODIFIER c.*689C>T| S205
15 BAA09g31790 A09 40102243 G A downstream_gene_variant MODIFIER c.*1139G>A| S105
S106
16 BAA09g31790 A09 40102612 C T downstream_gene_variant MODIFIER c.*1508C>T| S10
17 BAA09g31790 A09 40102892 C T downstream_gene_variant MODIFIER c.*1788C>T| S305
S36
18 BAA09g31790 A09 40103780 G T downstream_gene_variant MODIFIER c.*2676G>T| S189
19 BAA09g31790 A09 40104197 C T downstream_gene_variant MODIFIER c.*3093C>T| S230
20 BAA09g31790 A09 40104249 G A downstream_gene_variant MODIFIER c.*3145G>A| S150
21 BAA09g31790 A09 40104457 C T downstream_gene_variant MODIFIER c.*3353C>T| S293
22 BAA09g31790 A09 40104641 C T downstream_gene_variant MODIFIER c.*3537C>T| S236
23 BAA09g31790 A09 40105731 G A downstream_gene_variant MODIFIER c.*4627G>A| S268