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 BAA01g04660 A01 2064958 C T upstream_gene_variant MODIFIER c.-3216C>T| S18
2 BAA01g04660 A01 2066153 C T upstream_gene_variant MODIFIER c.-2021C>T| S235
S236
S260
3 BAA01g04660 A01 2066409 G A upstream_gene_variant MODIFIER c.-1765G>A| S234
4 BAA01g04660 A01 2066703 C T upstream_gene_variant MODIFIER c.-1471C>T| S117
5 BAA01g04660 A01 2066829 G A upstream_gene_variant MODIFIER c.-1345G>A| S295
6 BAA01g04660 A01 2067050 G A upstream_gene_variant MODIFIER c.-1124G>A| S13
7 BAA01g04660 A01 2068922 C T splice_region_variant&intron_variant LOW c.538-3C>T| S1
S90
8 BAA01g04660 A01 2070247 G A downstream_gene_variant MODIFIER c.*486G>A| S11
9 BAA01g04660 A01 2070607 G A downstream_gene_variant MODIFIER c.*846G>A| S169
10 BAA01g04660 A01 2070656 G A downstream_gene_variant MODIFIER c.*895G>A| S178
11 BAA01g04660 A01 2070689 G A downstream_gene_variant MODIFIER c.*928G>A| S271
12 BAA01g04660 A01 2071225 C T downstream_gene_variant MODIFIER c.*1464C>T| S240
13 BAA01g04660 A01 2071627 G A downstream_gene_variant MODIFIER c.*1866G>A| S298
14 BAA01g04660 A01 2073860 C T downstream_gene_variant MODIFIER c.*4099C>T| S267