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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g10470 A02 4638121 G A upstream_gene_variant MODIFIER c.-4204G>A| S206
S26
2 BAA02g10470 A02 4638619 G A upstream_gene_variant MODIFIER c.-3706G>A| S205
3 BAA02g10470 A02 4638703 G A upstream_gene_variant MODIFIER c.-3622G>A| S7
4 BAA02g10470 A02 4638953 C T upstream_gene_variant MODIFIER c.-3372C>T| S250
5 BAA02g10470 A02 4639429 G A upstream_gene_variant MODIFIER c.-2896G>A| S298
6 BAA02g10470 A02 4639958 C T upstream_gene_variant MODIFIER c.-2367C>T| S243
7 BAA02g10470 A02 4643095 G A missense_variant MODERATE c.85G>A|p.Glu29Lys S282
8 BAA02g10470 A02 4643835 C T missense_variant MODERATE c.422C>T|p.Ala141Val S186
9 BAA02g10470 A02 4644849 C T missense_variant MODERATE c.950C>T|p.Ala317Val S270
10 BAA02g10470 A02 4646073 G A downstream_gene_variant MODIFIER c.*478G>A| S47
11 BAA02g10470 A02 4646293 C T downstream_gene_variant MODIFIER c.*698C>T| S200
12 BAA02g10470 A02 4646714 C T downstream_gene_variant MODIFIER c.*1119C>T| S63
13 BAA02g10470 A02 4647098 C T downstream_gene_variant MODIFIER c.*1503C>T| S76
14 BAA02g10470 A02 4647283 C T downstream_gene_variant MODIFIER c.*1688C>T| S38