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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g16110 A05 8862792 C T upstream_gene_variant MODIFIER c.-4674C>T| S12
2 BAA05g16110 A05 8863366 C T upstream_gene_variant MODIFIER c.-4100C>T| S259
3 BAA05g16110 A05 8863368 T C upstream_gene_variant MODIFIER c.-4098T>C| S139
4 BAA05g16110 A05 8863760 C T upstream_gene_variant MODIFIER c.-3706C>T| S205
5 BAA05g16110 A05 8863868 C T upstream_gene_variant MODIFIER c.-3598C>T| S140
S278
S279
6 BAA05g16110 A05 8863939 G A upstream_gene_variant MODIFIER c.-3527G>A| S294
7 BAA05g16110 A05 8864336 C T upstream_gene_variant MODIFIER c.-3130C>T| S167
8 BAA05g16110 A05 8864881 C T upstream_gene_variant MODIFIER c.-2585C>T| S191
9 BAA05g16110 A05 8864897 G A upstream_gene_variant MODIFIER c.-2569G>A| S76
10 BAA05g16110 A05 8866109 G A upstream_gene_variant MODIFIER c.-1357G>A| S238
11 BAA05g16110 A05 8866954 C T upstream_gene_variant MODIFIER c.-512C>T| S47
12 BAA05g16110 A05 8867512 G A missense_variant MODERATE c.47G>A|p.Gly16Glu S187
13 BAA05g16110 A05 8868546 C T missense_variant MODERATE c.982C>T|p.Leu328Phe S182
14 BAA05g16110 A05 8869706 C T synonymous_variant LOW c.2073C>T|p.Phe691Phe S36
15 BAA05g16110 A05 8869845 C T missense_variant MODERATE c.2212C>T|p.Pro738Ser S71
16 BAA05g16110 A05 8869865 C T synonymous_variant LOW c.2232C>T|p.Phe744Phe S88
17 BAA05g16110 A05 8872284 G A downstream_gene_variant MODIFIER c.*2266G>A| S122
18 BAA05g16110 A05 8872513 C T downstream_gene_variant MODIFIER c.*2495C>T| S9