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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g16630 A02 8178491 C T missense_variant MODERATE c.952G>A|p.Gly318Arg S12
2 BAA02g16630 A02 8178787 C T synonymous_variant LOW c.810G>A|p.Leu270Leu S255
3 BAA02g16630 A02 8180681 A G upstream_gene_variant MODIFIER c.-725T>C| S18
4 BAA02g16630 A02 8180734 C T upstream_gene_variant MODIFIER c.-778G>A| S58
5 BAA02g16630 A02 8180938 C T upstream_gene_variant MODIFIER c.-982G>A| S32
6 BAA02g16630 A02 8181475 G A upstream_gene_variant MODIFIER c.-1519C>T| S23
7 BAA02g16630 A02 8181664 C T upstream_gene_variant MODIFIER c.-1708G>A| S164
8 BAA02g16630 A02 8182405 G A upstream_gene_variant MODIFIER c.-2449C>T| S282
9 BAA02g16630 A02 8182550 G A upstream_gene_variant MODIFIER c.-2594C>T| S135
10 BAA02g16630 A02 8183309 G A upstream_gene_variant MODIFIER c.-3353C>T| S247
11 BAA02g16630 A02 8183384 G A upstream_gene_variant MODIFIER c.-3428C>T| S69
12 BAA02g16630 A02 8183471 G A upstream_gene_variant MODIFIER c.-3515C>T| S187
13 BAA02g16630 A02 8183724 G A upstream_gene_variant MODIFIER c.-3768C>T| S168
S84
S93
14 BAA02g16630 A02 8183932 C T upstream_gene_variant MODIFIER c.-3976G>A| S211
15 BAA02g16630 A02 8184014 C T upstream_gene_variant MODIFIER c.-4058G>A| S58