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


Gene ID

Results: 1 - 31 of 31 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g42690 A02 35526777 C T upstream_gene_variant MODIFIER c.-4438C>T| S157
2 BAA02g42690 A02 35527261 C T upstream_gene_variant MODIFIER c.-3954C>T| S32
3 BAA02g42690 A02 35528454 G A upstream_gene_variant MODIFIER c.-2761G>A| S187
4 BAA02g42690 A02 35528475 C T upstream_gene_variant MODIFIER c.-2740C>T| S256
5 BAA02g42690 A02 35528675 C T upstream_gene_variant MODIFIER c.-2540C>T| S9
6 BAA02g42690 A02 35528791 G A upstream_gene_variant MODIFIER c.-2424G>A| S210
7 BAA02g42690 A02 35529170 C T upstream_gene_variant MODIFIER c.-2045C>T| S270
8 BAA02g42690 A02 35529246 G A upstream_gene_variant MODIFIER c.-1969G>A| S184
9 BAA02g42690 A02 35529368 C T upstream_gene_variant MODIFIER c.-1847C>T| S6
10 BAA02g42690 A02 35530190 C T upstream_gene_variant MODIFIER c.-1025C>T| S6
11 BAA02g42690 A02 35530637 G A upstream_gene_variant MODIFIER c.-578G>A| S210
12 BAA02g42690 A02 35531120 C T upstream_gene_variant MODIFIER c.-95C>T| S242
13 BAA02g42690 A02 35531609 C T intron_variant MODIFIER c.172-68C>T| S17
14 BAA02g42690 A02 35531852 C T intron_variant MODIFIER c.234+113C>T| S48
15 BAA02g42690 A02 35532666 G A intron_variant MODIFIER c.235-178G>A| S281
16 BAA02g42690 A02 35532929 G A missense_variant MODERATE c.320G>A|p.Arg107Lys S213
17 BAA02g42690 A02 35532934 G A splice_donor_variant&intron_variant HIGH c.324+1G>A| S166
18 BAA02g42690 A02 35534607 C T intron_variant MODIFIER c.516+1103C>T| S153
S213
19 BAA02g42690 A02 35536591 T C intron_variant MODIFIER c.750+45T>C| S54
20 BAA02g42690 A02 35536607 G A intron_variant MODIFIER c.751-48G>A| S134
21 BAA02g42690 A02 35538446 C T downstream_gene_variant MODIFIER c.*64C>T| S173
22 BAA02g42690 A02 35538653 C T downstream_gene_variant MODIFIER c.*271C>T| S242
23 BAA02g42690 A02 35539442 G A downstream_gene_variant MODIFIER c.*1060G>A| S282
24 BAA02g42690 A02 35540544 G A downstream_gene_variant MODIFIER c.*2162G>A| S199
25 BAA02g42690 A02 35541313 A C downstream_gene_variant MODIFIER c.*2931A>C| S12