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


Gene ID

Results: 1 - 24 of 24 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA04g00430 A04 276295 G A downstream_gene_variant MODIFIER c.*4750C>T| S40
S49
2 BAA04g00430 A04 276406 G A downstream_gene_variant MODIFIER c.*4639C>T| S190
3 BAA04g00430 A04 276858 C T downstream_gene_variant MODIFIER c.*4187G>A| S158
4 BAA04g00430 A04 277547 G A downstream_gene_variant MODIFIER c.*3498C>T| S190
5 BAA04g00430 A04 278079 C T downstream_gene_variant MODIFIER c.*2966G>A| S178
6 BAA04g00430 A04 279366 C T downstream_gene_variant MODIFIER c.*1679G>A| S231
7 BAA04g00430 A04 280153 C T downstream_gene_variant MODIFIER c.*892G>A| S202
8 BAA04g00430 A04 280669 C T downstream_gene_variant MODIFIER c.*376G>A| S233
9 BAA04g00430 A04 280686 C T downstream_gene_variant MODIFIER c.*359G>A| S231
10 BAA04g00430 A04 281388 C T missense_variant MODERATE c.125G>A|p.Arg42Lys S278
S279
11 BAA04g00430 A04 282088 G A upstream_gene_variant MODIFIER c.-375C>T| S251
12 BAA04g00430 A04 282228 G A upstream_gene_variant MODIFIER c.-515C>T| S142
13 BAA04g00430 A04 282247 G A upstream_gene_variant MODIFIER c.-534C>T| S127
14 BAA04g00430 A04 282378 G A upstream_gene_variant MODIFIER c.-665C>T| S167
15 BAA04g00430 A04 282595 C T upstream_gene_variant MODIFIER c.-882G>A| S35
16 BAA04g00430 A04 282662 C T upstream_gene_variant MODIFIER c.-949G>A| S5
17 BAA04g00430 A04 282678 G A upstream_gene_variant MODIFIER c.-965C>T| S120
18 BAA04g00430 A04 284518 C T upstream_gene_variant MODIFIER c.-2805G>A| S277
S66
19 BAA04g00430 A04 284806 C T upstream_gene_variant MODIFIER c.-3093G>A| S46
20 BAA04g00430 A04 285116 G A upstream_gene_variant MODIFIER c.-3403C>T| S155
21 BAA04g00430 A04 285226 G A upstream_gene_variant MODIFIER c.-3513C>T| S136
22 BAA04g00430 A04 285845 G A upstream_gene_variant MODIFIER c.-4132C>T| S36
23 BAA04g00430 A04 285998 C T upstream_gene_variant MODIFIER c.-4285G>A| S1
S90
24 BAA04g00430 A04 286605 G A upstream_gene_variant MODIFIER c.-4892C>T| S162