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 BAA03g53460 A03 26338061 C T upstream_gene_variant MODIFIER c.-4751C>T| S293
2 BAA03g53460 A03 26338174 C T upstream_gene_variant MODIFIER c.-4638C>T| S183
S198
3 BAA03g53460 A03 26338369 G A upstream_gene_variant MODIFIER c.-4443G>A| S203
4 BAA03g53460 A03 26340088 C T upstream_gene_variant MODIFIER c.-2724C>T| S113
5 BAA03g53460 A03 26340184 C T upstream_gene_variant MODIFIER c.-2628C>T| S9
6 BAA03g53460 A03 26340505 C T upstream_gene_variant MODIFIER c.-2307C>T| S270
7 BAA03g53460 A03 26340559 G A upstream_gene_variant MODIFIER c.-2253G>A| S265
8 BAA03g53460 A03 26340666 G A upstream_gene_variant MODIFIER c.-2146G>A| S296
9 BAA03g53460 A03 26340673 G A upstream_gene_variant MODIFIER c.-2139G>A| S84
S93
10 BAA03g53460 A03 26342017 G A upstream_gene_variant MODIFIER c.-795G>A| S174
S265
S27
11 BAA03g53460 A03 26342226 C T upstream_gene_variant MODIFIER c.-586C>T| S234
12 BAA03g53460 A03 26342418 C T upstream_gene_variant MODIFIER c.-394C>T| S121
13 BAA03g53460 A03 26342836 G A missense_variant MODERATE c.25G>A|p.Gly9Ser S272
14 BAA03g53460 A03 26344824 C T synonymous_variant LOW c.939C>T|p.Arg313Arg S42