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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA04g06790 A04 4494615 C T upstream_gene_variant MODIFIER c.-376C>T| S80
2 BAA04g06790 A04 4494976 C T upstream_gene_variant MODIFIER c.-15C>T| S294
3 BAA04g06790 A04 4495548 C T intron_variant MODIFIER c.317+87C>T| S249
4 BAA04g06790 A04 4495715 C T intron_variant MODIFIER c.318-128C>T| S207
5 BAA04g06790 A04 4498355 G A missense_variant MODERATE c.1183G>A|p.Ala395Thr S217
S248
6 BAA04g06790 A04 4498617 G A intron_variant MODIFIER c.1240-56G>A| S201
7 BAA04g06790 A04 4498835 G A splice_acceptor_variant&intron_variant HIGH c.1325-1G>A| S177
8 BAA04g06790 A04 4499700 C T downstream_gene_variant MODIFIER c.*3C>T| S187
9 BAA04g06790 A04 4499864 G A downstream_gene_variant MODIFIER c.*167G>A| S103
10 BAA04g06790 A04 4499989 C T downstream_gene_variant MODIFIER c.*292C>T| S249
11 BAA04g06790 A04 4501206 G A downstream_gene_variant MODIFIER c.*1509G>A| S94
12 BAA04g06790 A04 4502066 G A downstream_gene_variant MODIFIER c.*2369G>A| S52
13 BAA04g06790 A04 4502249 G A downstream_gene_variant MODIFIER c.*2552G>A| S183
S198
14 BAA04g06790 A04 4502360 C T downstream_gene_variant MODIFIER c.*2663C>T| S118
15 BAA04g06790 A04 4502603 G A downstream_gene_variant MODIFIER c.*2906G>A| S295
16 BAA04g06790 A04 4503207 C T downstream_gene_variant MODIFIER c.*3510C>T| S73
S91