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


Gene ID

Results: 1 - 26 of 26 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA04g08460 A04 5822768 G A upstream_gene_variant MODIFIER c.-4713G>A| S11
2 BAA04g08460 A04 5824912 G A upstream_gene_variant MODIFIER c.-2569G>A| S57
3 BAA04g08460 A04 5825180 G T upstream_gene_variant MODIFIER c.-2301G>T| S135
4 BAA04g08460 A04 5825199 C T upstream_gene_variant MODIFIER c.-2282C>T| S2
5 BAA04g08460 A04 5825275 G A upstream_gene_variant MODIFIER c.-2206G>A| S25
6 BAA04g08460 A04 5825318 G A upstream_gene_variant MODIFIER c.-2163G>A| S150
7 BAA04g08460 A04 5825413 C T upstream_gene_variant MODIFIER c.-2068C>T| S296
8 BAA04g08460 A04 5825619 G A upstream_gene_variant MODIFIER c.-1862G>A| S273
9 BAA04g08460 A04 5825720 C T upstream_gene_variant MODIFIER c.-1761C>T| S192
10 BAA04g08460 A04 5825772 C A upstream_gene_variant MODIFIER c.-1709C>A| S170
S185
S197
S204
S240
S244
11 BAA04g08460 A04 5825924 C T upstream_gene_variant MODIFIER c.-1557C>T| S100
12 BAA04g08460 A04 5827204 C T upstream_gene_variant MODIFIER c.-277C>T| S1
13 BAA04g08460 A04 5827631 G A missense_variant MODERATE c.151G>A|p.Val51Ile S126
14 BAA04g08460 A04 5828293 G A missense_variant&splice_region_variant MODERATE c.787G>A|p.Asp263Asn S303
15 BAA04g08460 A04 5828422 G A intron_variant MODIFIER c.788+128G>A| S28
16 BAA04g08460 A04 5828554 C T intron_variant MODIFIER c.788+260C>T| S32
17 BAA04g08460 A04 5828624 C T intron_variant MODIFIER c.788+330C>T| S205
18 BAA04g08460 A04 5828806 C T intron_variant MODIFIER c.788+512C>T| S208
S93
19 BAA04g08460 A04 5829793 C T intron_variant MODIFIER c.788+1499C>T| S271
20 BAA04g08460 A04 5830176 G A intron_variant MODIFIER c.788+1882G>A| S133
21 BAA04g08460 A04 5830292 G A intron_variant MODIFIER c.788+1998G>A| S121
22 BAA04g08460 A04 5830504 T A intron_variant MODIFIER c.788+2210T>A| S62
23 BAA04g08460 A04 5831563 G A intron_variant MODIFIER c.788+3269G>A| S40
S49
24 BAA04g08460 A04 5831840 G A intron_variant MODIFIER c.788+3546G>A| S71
25 BAA04g08460 A04 5837003 C T missense_variant MODERATE c.965C>T|p.Ser322Phe S53