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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g25210 A09 16182471 G A downstream_gene_variant MODIFIER c.*4446C>T| S51
2 BAA09g25210 A09 16182631 G A downstream_gene_variant MODIFIER c.*4286C>T| S129
3 BAA09g25210 A09 16182720 C T downstream_gene_variant MODIFIER c.*4197G>A| S4
4 BAA09g25210 A09 16182841 G A downstream_gene_variant MODIFIER c.*4076C>T| S245
5 BAA09g25210 A09 16183001 G A downstream_gene_variant MODIFIER c.*3916C>T| S66
6 BAA09g25210 A09 16183127 G A downstream_gene_variant MODIFIER c.*3790C>T| S217
S248
7 BAA09g25210 A09 16183575 C T downstream_gene_variant MODIFIER c.*3342G>A| S264
8 BAA09g25210 A09 16183925 C T downstream_gene_variant MODIFIER c.*2992G>A| S153
9 BAA09g25210 A09 16184313 G A downstream_gene_variant MODIFIER c.*2604C>T| S172
S217
10 BAA09g25210 A09 16184314 G A downstream_gene_variant MODIFIER c.*2603C>T| S34
11 BAA09g25210 A09 16184363 G A downstream_gene_variant MODIFIER c.*2554C>T| S236
12 BAA09g25210 A09 16184632 C T downstream_gene_variant MODIFIER c.*2285G>A| S233
13 BAA09g25210 A09 16185432 C T downstream_gene_variant MODIFIER c.*1485G>A| S133
S55
14 BAA09g25210 A09 16187048 C T missense_variant MODERATE c.442G>A|p.Glu148Lys S176
15 BAA09g25210 A09 16187514 G A upstream_gene_variant MODIFIER c.-25C>T| S57
16 BAA09g25210 A09 16188105 G A upstream_gene_variant MODIFIER c.-616C>T| S77
S82
17 BAA09g25210 A09 16188145 G A upstream_gene_variant MODIFIER c.-656C>T| S196
18 BAA09g25210 A09 16189152 C T upstream_gene_variant MODIFIER c.-1663G>A| S156
19 BAA09g25210 A09 16189291 G A upstream_gene_variant MODIFIER c.-1802C>T| S74
20 BAA09g25210 A09 16192099 G A upstream_gene_variant MODIFIER c.-4610C>T| S176