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 BAA07g00010 A07 290 C T upstream_gene_variant MODIFIER c.-3286C>T| S52
2 BAA07g00010 A07 297 C T upstream_gene_variant MODIFIER c.-3279C>T| S34
3 BAA07g00010 A07 883 C T upstream_gene_variant MODIFIER c.-2693C>T| S250
4 BAA07g00010 A07 1073 C T upstream_gene_variant MODIFIER c.-2503C>T| S247
5 BAA07g00010 A07 1256 G A upstream_gene_variant MODIFIER c.-2320G>A| S51
6 BAA07g00010 A07 1298 G A upstream_gene_variant MODIFIER c.-2278G>A| S202
7 BAA07g00010 A07 1578 C T upstream_gene_variant MODIFIER c.-1998C>T| S124
8 BAA07g00010 A07 1969 C T upstream_gene_variant MODIFIER c.-1607C>T| S287
9 BAA07g00010 A07 2412 C T upstream_gene_variant MODIFIER c.-1164C>T| S247
10 BAA07g00010 A07 2996 C T upstream_gene_variant MODIFIER c.-580C>T| S270
11 BAA07g00010 A07 3110 G A upstream_gene_variant MODIFIER c.-466G>A| S273
12 BAA07g00010 A07 3498 G A upstream_gene_variant MODIFIER c.-78G>A| S105
S106
13 BAA07g00010 A07 3849 G A missense_variant MODERATE c.188G>A|p.Gly63Glu S30
S31
14 BAA07g00010 A07 4054 C T intron_variant MODIFIER c.373+20C>T| S178
15 BAA07g00010 A07 4586 C T missense_variant MODERATE c.766C>T|p.Pro256Ser S42
16 BAA07g00010 A07 4850 C T downstream_gene_variant MODIFIER c.*238C>T| S178
17 BAA07g00010 A07 4857 C T downstream_gene_variant MODIFIER c.*245C>T| S42
18 BAA07g00010 A07 4990 G A downstream_gene_variant MODIFIER c.*378G>A| S78
19 BAA07g00010 A07 5292 C A downstream_gene_variant MODIFIER c.*680C>A| S244
S248
S279
S283
S305
S62
S89
20 BAA07g00010 A07 5519 C T downstream_gene_variant MODIFIER c.*907C>T| S18
21 BAA07g00010 A07 5779 G A downstream_gene_variant MODIFIER c.*1167G>A| S202
22 BAA07g00010 A07 5924 C T downstream_gene_variant MODIFIER c.*1312C>T| S28
23 BAA07g00010 A07 6041 G A downstream_gene_variant MODIFIER c.*1429G>A| S263